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Copper iodide (CuI) has garnered considerable attention as a promising alternative to p‐type transparent conducting oxides owing to its low cation vacancy formation energy, shallow acceptor level, and readily modifiable conductivity via doping. Although sulfur (S) doping through liquid iodination has exhibited high efficacy in enhancing the conductivity with record high figure of merit (FOM) of 630 00 MΩ−1, solution‐processed S‐doped CuI (CuI:S) for low‐cost large area fabrication has yet to be explored. Here, a highly conducting CuI:S thin‐film for p‐type transparent conducting electrode (TCE) is reported using low temperature solution‐processing with thiourea derivatives. The optimization of thiourea dopant is determined through a comprehensive acid‐base study, considering the effects of steric hindrance. The modification of active groups of thioureas facilitated a varying carrier concentration range of 9 × 1018–2.52 × 1020 cm−3 and conductivities of 4.4–390.7 S cm−1. Consequently, N‐ethylthiourea‐doped CuI:S exhibited a FOM value of 7 600 MΩ−1, which is the highest value among solution‐processed p‐type TCEs to date. Moreover, the formulation of CuI:S solution for highly conductive p‐type TCEs can be extended to CuI:S inks, facilitating high‐throughput solution‐processes such as inkjet printing and spray coating. [ABSTRACT FROM AUTHOR]

The photoluminescence (PL) of cuprous iodide (CuI) has drawn significant attention in the scientific community. In order to investigate the growth methods and environmental conditions on the fluorescence, we first prepared CuI via immersion of copper in hydroiodic acid. This method is beneficial for the growth of large grains (> 20 μm) with intensive red fluorescence emission at 708 nm. The fluorescence has a high quantum yield (34 %), and superior stability. Then we studied the fluorescence behaviors in water. We observed fluorescence quenching, which is due to the energy transfer. Additionally, we studied the effect of temperature on the fluorescence. We found that the fluorescence intensity increased initially then decreased as the temperature increased. The underlying mechanism was analyzed in terms of fluorescence quencher (water) removal and thermal quenching. By controlling heating, we successfully obtained intensive and pure red fluorescence. Finally, we explored the potential application of the red fluorescent of CuI in optical communication. The results demonstrate bit error rates within permissible range of forward error correction, highlighting the superior performance of CuI in optical communication systems. [ABSTRACT FROM AUTHOR]

To tailor electrical properties of often degenerate pristine CuI, Ni is introduced as alloy constituent. Cosputtering in a reactive, but also in an inert atmosphere as well as pulsed laser deposition (PLD), is used to grow NixCu1−xI$\left(\text{Ni}\right)_{x} \left(\text{Cu}\right)_{1 - x} \text{I}$ thin films. The Ni content within the alloy thin films is systematically varied for different growth techniques and growth conditions. A solubility limit is evidenced by an additional NiI2(H2O)6$\left(\text{NiI}\right)_{2} \left(\left(\text{(H}\right)_{2} \text{O)}\right)_{6}$ phase for Ni contents x≥0.31$x \geq 0.31$, observed in X‐Ray diffraction and atomic force microscopy by a change in surface morphology. Furthermore, metallic, nanoscaled nickel clusters, revealed by X‐Ray photoelectron spectroscopy and high‐resolution transmission electron microscopy (HRTEM), underpin a solubility limit of Ni in CuI. Although no reduction of charge carrier density is observed with increasing Ni content, a dilute magnetic behavior of the thin films is observed in vibrating sample magnetometry. Further, independent of the deposition technique, unique multilayer features are observed in HRTEM measurements for thin films of a cation composition of x≈0.06$x \approx $. Opposite to previous claims, no transition to n‐type behavior was observed, which was also confirmed by density functional theory calculations of the alloy system. [ABSTRACT FROM AUTHOR]

Starting from readily available enantiopure azidomethyl‐substituted bicyclic 1,2‐oxazine derivatives and mono‐, di‐ or trialkynes, their copper‐catalyzed (3+2) cycloadditions furnished a series of 1,2,3‐triazolyl‐linked compounds in good yields. These click reactions proceeded smoothly at room temperature when copper iodide as catalyst was used in the presence of triethylamine and tris[(1‐gbenzyl‐1H‐1,2,3‐triazol‐4‐yl)methyl]amine as ligand. Generally, the unprotected bicyclic 1,2‐oxazine derivatives seemed to show slightly higher reactivity and provided better yields compared with their silyl‐protected counterparts. Exhaustive hydrogenolysis with cleavage of the 1,2‐oxazine N−O bonds in the presence of palladium on charcoal as promotor is feasible but was found to be capricious. Reasonable results were obtained when acetic acid was employed as cosolvent. By applying these conditions, several of the bicyclic 1,2‐oxazine derivatives were successfully converted into the expected mono‐ or divalent aminooxepine derivatives which can be regarded as aminoseptanose mimetics. [ABSTRACT FROM AUTHOR]

As a new inorganic lead‐free perovskite, cesium copper iodide (CsCu2I3) has attracted wide attention in the field of photodetectors due to its non‐toxicity, good air and thermal stability, and excellent optoelectronic properties. However, the random growth and disordered distribution of CsCu2I3 crystals during their preparation results in poor crystal quality, seriously limiting their applications. Highly ordered CsCu2I3 crystal formation with high crystal quality for high‐performance photodetectors remains a major challenge. Here, an ingenious nanoimprinting technology is utilized to obtain high‐performance photodetectors based on highly aligned CsCu2I3 nanowires (NWs). Owing to the high crystal quality, the photodetector exhibits excellent responsivity of 12.35 A W−1 (310 nm) and 89.73 mA W−1 (365 nm), respectively, as well as good polarization light detection with a dichroism ratio of up to 2.28. Additionally, the device on a flexible substrate retains its initial level of performance even after being bent 2000 times. Remarkably, the device exhibits superior stability and maintains excellent performance after being placed in the natural environment for 1 month without any encapsulation. [ABSTRACT FROM AUTHOR]

In recent years, tin halide perovskite solar cells (PKSCs) have emerged as a promising alternative to lead‐PKSCs. However, due to defects such as Sn4+ and iodide vacancies, their efficiency is lower than lead‐PKSCs. To address this issue, various strategies are proposed to improve the quality of perovskite, including copper iodide (CuI) doping. Unfortunately, the conventional solvent composition of DMF:DMSO = 4:1 has limited the solubility of CuI, resulting in inconsistent results and limited efficiency improvements. However, this research proposed a preprocessing method of CuI to decrease the defects and improve the perovskite layer's morphology. As a result, the efficiency of tin‐PKSCs with both P‐I‐N and hole transport layer (HTL) free structures is enhanced, increasing from 9.8% to 13.1% and 9.4% to 10.5%, respectively. Moreover, the doped tin‐PKSCs have exhibited better stability, retaining 75% of their initial power conversion efficiency (PCE) after being stored in a glovebox for 102 days. [ABSTRACT FROM AUTHOR]

The long‐term stability of the optically transparent p‐type semiconductor copper iodide is a current challenge. The electrical conductivity of CuI thin films depends critically on the environmental impact. Al2O3 cappings enhance the stability considerably. Systematic studies on Al2O3/CuI heterostructures in dependence of the N2/O2 growth pressure show the electrical conductivity of the CuI films being determined by the oxygen diffusion through Al2O3 und CuI. Oxygen seems to be a dominating acceptor in CuI. We traced the diffusion of atmospheric oxygen into CuI with 18O isotopes. [ABSTRACT FROM AUTHOR]

Chiral hybrid Cu(I)‐based iodides with d10 closed shell demonstrate great potential for circularly polarized luminescence (CPL) because of high photoluminescence quantum yield (PLQY). Herein, by incorporating mono‐ or bi‐dentate coordination mode ligands as chiral source, the self‐assembly of four pairs of chiral hybrid Cu(I)‐based iodides, namely, (R/S)‐Cu4I4(Hmpy)4·H2O (R/S‐1), (R/S)‐Cu4I4(3Hpy)4 (R/S‐2), (R/S)‐Cu4I4(2MePI)4 (R/S‐3), and (R/S)‐Cu4I4(3AD)4 (R/S‐4) (where R/S‐Hmpy = R/S‐2‐pyrrolidinemethanol, R/S‐3Hpy = R/S‐3‐hydroxypyrrolidine, R/S‐2MePI = R/S‐2‐methylpiperazine, and R/S‐3AD = R/S‐3‐aminopiperidine), are reported. With the monodentate and bidentate ligands, these materials belong to two different structural types: 0D molecular clusters (R/S‐1, R/S‐2) and 3D porous metal–organic frameworks (R/S‐3, R/S‐4). These materials all crystallize in non‐centrosymmetric space groups containing similar basic Cu4I4 cubane tetramer building units but with different coordination modes. They are also semiconductors, with optical bandgaps ranging from 2.70 to 2.94 eV. The photoluminescence (PL) and circularly polarized luminescence (CPL) emissions are further characterized, where the highest PLQY of ≈95% and CPL dissymmetry factor (glum) of ≈7 × 10−3 are achieved in R/S‐1. This work offers a systematic comparison between different structural types with similar building blocks, bridging by the flexible chiral ligands, and shows that the hybrid copper iodides are highly promising candidates for next‐generation optoelectronics and chiroptics. [ABSTRACT FROM AUTHOR]

X‐ray imaging technology has achieved important applications in many fields and has attracted extensive attentions. Dynamic X‐ray flexible imaging for the real‐time observation of the internal structure of complex materials is the most challenging type of X‐ray imaging technology, which requires high‐performance X‐ray scintillators with high X‐ray excited luminescence (XEL) efficiency as well as excellent processibility and stability. Here, a macrocyclic bridging ligand with aggregation‐induced emission (AIE) feature was introduced for constructing a copper iodide cluster‐based metal–organic framework (MOF) scintillator. This strategy endows the scintillator with high XEL efficiency and excellent chemical stability. Moreover, a regular rod‐like microcrystal was prepared through the addition of polyvinyl pyrrolidone during the in situ synthesis process, which further enhanced the XEL and processibility of the scintillator. The microcrystal was used for the preparation of a scintillator screen with excellent flexibility and stability, which can be used for high‐performance X‐ray imaging in extremely humid environments. Furthermore, dynamic X‐ray flexible imaging was realized for the first time. The internal structure of flexible objects was observed in real time with an ultrahigh resolution of 20 LP mm−1. [ABSTRACT FROM AUTHOR]

X‐ray imaging technology has achieved important applications in many fields and has attracted extensive attentions. Dynamic X‐ray flexible imaging for the real‐time observation of the internal structure of complex materials is the most challenging type of X‐ray imaging technology, which requires high‐performance X‐ray scintillators with high X‐ray excited luminescence (XEL) efficiency as well as excellent processibility and stability. Here, a macrocyclic bridging ligand with aggregation‐induced emission (AIE) feature was introduced for constructing a copper iodide cluster‐based metal–organic framework (MOF) scintillator. This strategy endows the scintillator with high XEL efficiency and excellent chemical stability. Moreover, a regular rod‐like microcrystal was prepared through the addition of polyvinyl pyrrolidone during the in situ synthesis process, which further enhanced the XEL and processibility of the scintillator. The microcrystal was used for the preparation of a scintillator screen with excellent flexibility and stability, which can be used for high‐performance X‐ray imaging in extremely humid environments. Furthermore, dynamic X‐ray flexible imaging was realized for the first time. The internal structure of flexible objects was observed in real time with an ultrahigh resolution of 20 LP mm−1. [ABSTRACT FROM AUTHOR]

Cyclotribenzylenes (CTBs) combining carbonitrile (−CN) and alkyne (−C2H) substituents were synthesized as racemic mixtures and resolved by HPLC on chiral stationary phases. Two of these compounds were used to prepare platinum‐bridged CTB dimers, in which PtII is bound to the CTBs via Pt−alkynyl bonds in cis configuration. The organometallic complexes were examined by mass spectrometry and NMR spectroscopy, which indicated that they were obtained as mixtures of diastereoisomers (a meso or syn form and a pair of chiral or anti forms) when racemic CTBs were used. Enantiomerically pure complexes were prepared from resolved CTBs, which allowed us to distinguish the NMR signals of the chiral and meso forms in the diastereoisomeric mixtures. In certain conditions, the platinum complexes played the role of a pincer π‐alkynyl ligand for Cu(I) coming from the copper iodide used as a synthetic auxiliary. The Cu+ cations could be easily removed by treatment with NaCN, affording the mononuclear bis‐cyclotribenzylene complexes. These compounds failed to lead to metallo‐cryptophanes by coordination of two [M(dppp)]2+ complex subunits (M=Pd, Pt; dppp=1,3‐bis(diphenylphosphino)propane), each to two carbonitrile substituents belonging to different CTBs, pointing to the superiority of the one pot self‐assembly processes for the preparation of metallo‐cryptophanes. [ABSTRACT FROM AUTHOR]

Copper iodide (CuI) thin films were prepared on a glass substrate by a facile high pressure (HP)‐PECVD method at room temperature. For this, CuI powder was dissolved in CH3CN. The CuI vapor with plasma was investigated by Optical Emission Spectroscopic (OES) data for identifying the species in the plasma. The XRD study reveals the polycrystalline nature of the films. The SEM analyses indicate the homogeneity of the films. The EDS mapping confirms that the thin films mostly consisted of carbon followed by nitrogen, copper and iodine, respectively. The band gaps of CuI thin films were in the range of ~2.71–3.14 eV. The high transmittance and band gap engineering in HP‐PECVD‐synthesized CuI thin films indicates their potential use as window and hole transport layers in low cost solar cells. [ABSTRACT FROM AUTHOR]

Nonradiative decays of surface plasmon (SP) can generate photocarriers in femtosecond, and it therefore has been attracting widespread research attention in ultrafast optoelectronics. Taking advantage of the probe technique, Kelvin probe force microscopy (KPFM) can characterize the spatial distribution of hot carriers in nanoscale and thereby provide necessary analysis for device investigation and engineering. In this work, the behavior of plasmonic hot holes is demonstrated for Ag nanoparticles (NPs) based on the fabrication of CuI hole transport layers. The morphological, optical, and electronic properties of Ag NPs and CuI films are systematically investigated. With the confocal lasers of over‐ and sub‐bandgap wavelength, reversed evolution trends of surface potentials are observed by KPFM, indicating the effective injection of hot holes into CuI valence band (VB). Cross‐verification is also performed based on the fabrication of metal–semiconductor–metal (MSM) photodetectors, and the photoelectrical tests highly dovetail with the surface potential evolution. This research provides an important reference for the plasmonic photoelectronics in both device design and research methods. [ABSTRACT FROM AUTHOR]

Transition‐metal‐catalyzed enantioselective P−C cross‐coupling of secondary phosphine oxides (SPOs) is an attractive method for synthesizing P‐stereogenic phosphorus compounds, but the development of such a dynamic kinetic asymmetric process remains a considerable challenge. Here we report an unprecedented highly enantioselective dynamic kinetic intermolecular P−C coupling of SPOs and aryl iodides catalyzed by copper complexes ligated by a finely modified chiral 1,2‐diamine ligand. The reaction tolerates a wide range of SPOs and aryl iodides, affording P‐stereogenic tertiary phosphine oxides (TPOs) in high yields and with good enantioselectivity (average 89.2 % ee). The resulting enantioenriched TPOs were transformed into structurally diverse P‐chiral scaffolds, which are highly valuable as ligands and catalysts in asymmetric synthesis. [ABSTRACT FROM AUTHOR]

Transition‐metal‐catalyzed enantioselective P−C cross‐coupling of secondary phosphine oxides (SPOs) is an attractive method for synthesizing P‐stereogenic phosphorus compounds, but the development of such a dynamic kinetic asymmetric process remains a considerable challenge. Here we report an unprecedented highly enantioselective dynamic kinetic intermolecular P−C coupling of SPOs and aryl iodides catalyzed by copper complexes ligated by a finely modified chiral 1,2‐diamine ligand. The reaction tolerates a wide range of SPOs and aryl iodides, affording P‐stereogenic tertiary phosphine oxides (TPOs) in high yields and with good enantioselectivity (average 89.2 % ee). The resulting enantioenriched TPOs were transformed into structurally diverse P‐chiral scaffolds, which are highly valuable as ligands and catalysts in asymmetric synthesis. [ABSTRACT FROM AUTHOR]

Due to the textured nature of random in‐plane orientation of sputtered γ‐CuI (111) thin films, the crystalline grains and grain boundaries (GBs) influence charge carrier transport. Herein, current probe atomic force microscopy (cp‐AFM) measurements for differentiation and correlation of these morphological features and their contribution to electrical conductivity are presented, thus showing a clear difference between the conductive behavior of grains and GBs. A localized high and linearly voltage‐dependent current at the boundaries as well as a rectifying behavior between the platinum‐coated AFM tip and the grain surfaces is observed. Also, a different temporal evolution of voltage‐dependent conductivity is observed for grains and GBs. Further, the charge carrier transport through the surface vanishes with time. It is suspected that atmospheric oxygen causes these time‐dependent surface changes because accelerated degradation of the conductivity after oxygen plasma treatment is also measured. [ABSTRACT FROM AUTHOR]

Low-dimensional ternary copper iodide metal halide with strong quantum confinement effects has made great progress in optoelectronic fields. However, efficient regulation of anisotropic growth of metal halides single crystal still remains a great challenge. Herein, 2 cm size CsCu2I3 single crystals with tunable aspect ratio and the trap states (ntrap) as low as 5.38 X 109 cm-3 are fabricated by optimized anti-solvent vapor-assisted method, in which the growth cycle is shortened by half. Evidenced by real-time observation and the LaMer growth model, the rapid and anisotropic growth mechanism is ascribed to preferential 1D growth, promoted by high concentration and fast vapor rate. Furthermore, the aspect-ratio-dependent optoelectronic performance is observed, the on-off ratio for 2 cm CsCu2I3 single crystal are enhanced 350 times compared with those of short and thick single crystal, which shows ultrahigh on-off ratio of 1570, D* of 1.34 X 1012 Jones, RÁ of276.94 mA W-1, t rise /t decay of 0.37 and 1.08 ms, and EQE of95.53%, which are clearly at very high level among lead-free perovskite-based photodetectors. This study not only provides a new strategy for overcoming anisotropic growth limitations of low-dimensional metal halides, but also paves a way for high-performance optoelectronic applications. [ABSTRACT FROM AUTHOR]

This study demonstrates the efficacy of an emerging p‐type copper iodide (CuI) semiconductor in a flexible, low‐voltage resistive random‐access memory (RRAM), which can be readily integrated with metal‐oxide n‐type counterparts for complementary circuit systems. Herein, CuI RRAM devices are implemented via a room‐temperature solid iodination process, exhibiting a consistent On/Off ratio (≈104), excellent endurance of more than ≈103 cycles, together with a long retention period (> 5 × 104 s). Furthermore, a scheme of light‐mediated multi‐level data storage is demonstrated using blue light illumination (λ = 455 nm), to exploit possible photonic memristive functionality through notable photo‐response of CuI. In addition, the current conduction and resistive switching behaviors are systematically studied via low‐temperature measurements from 203 to 343 K, validating thermal stability and the governing key switching mechanism in CuI RRAM devices. The longstanding problem with CuI device longevity is effectively addressed via PMMA encapsulation, resulting in a 15‐fold improvement in the lifespan of devices even in air, as compared with non‐passivated devices. These findings suggest that flexible optoelectronic systems, combined with reliable, ultra‐low power CuI RRAM devices with photo memristive functionality, can leverage the enhancement of multifunctional selectors required in process‐in‐memories and the synaptic elements of neuromorphic applications. [ABSTRACT FROM AUTHOR]

The search for color‐tunable, efficient, and robust scintillators plays a vital role in the development of modern X‐ray radiography. The radioluminescence tuning of copper iodide cluster scintillators in the entire visible region by bandgap engineering is herein reported. The bandgap engineering benefits from the fact that the conduction band minimum and valence band maximum of copper iodide cluster crystals are contributed by atomic orbitals from the inorganic core and organic ligand components, respectively. In addition to high scintillation performance, the as‐prepared crystalline copper iodide cluster solids exhibit remarkable resistance toward both moisture and X‐ray irradiation. These features allow copper iodide cluster scintillators to show particular attractiveness for low‐dose X‐ray radiography with a detection limit of 55 nGy s−1, a value ≈100 times lower than a standard dosage for X‐ray examinations. The results suggest that optimizing both inorganic core and organic ligand for the building blocks of metal halide cluster crystals may provide new opportunities for a new generation of high‐performance scintillation materials. [ABSTRACT FROM AUTHOR]

Cyanodithioformate salt as an odorless and simply operational source of sulfur was reacted with aryl halides in the presence of copper iodide, affording diaryl disulfide, which reacted with styrenes/α‐methylstyrene in second step to form β‐Hydroxy sulfides with high regioselectivity in good to excellent yields. [ABSTRACT FROM AUTHOR]

Highly photoluminescent, lead‐free perovskites are of interest for displays and solid‐state light‐emitting devices. In this report, streak camera‐based time‐resolved emission and transient absorption spanning visible to deep‐ultraviolet (UV) wavelengths are utilized to study self‐trapped and free exciton dynamics in vacuum‐deposited cesium copper halide thin films of CsCu2I3 and Cs3Cu2I5. Self‐trapped exciton emission of CsCu2I3 exhibits more noticeable changes with time in the peak position and width than Cs3Cu2I5. UV‐to‐blue emission is detectable for both compositions, where free exciton emission is distinct for CsCu2I3. Transient absorption shows loss of ground‐state bleach signals at early time delays for both, and the bleach signal shifts toward higher energy as time delay increases, likely due to strains induced by the newly created self‐trapped excitons. Global analysis performed on the transient absorption results yields time constants in these materials that build an overall dynamic scheme. This work aids in building a complete picture regarding light emission in these promising materials. [ABSTRACT FROM AUTHOR]

Copper iodide (CuI) is a promising material for use as hole‐transport layers in electronic devices due to their solution processability and efficient hole conductivity. CuI has a rich chemistry with halide salts and solvents to which it may be exposed during device fabrication. Thus, care must be taken during device fabrication when CuI is used. We present a study using CuI as a hole transport layer in a p‐i‐n perovskite photovoltaic architecture. We studied how each of the components present in the perovskite precursor solution impacts the integrity of CuI films using power x‐ray diffraction, UV‐vis spectroscopy and impedance spectroscopy. Based on these studies, we show that DMSO, mixtures of γ‐butyrolactone:DMSO (v/v 7 : 3) and DMF:DMSO (v/v 8 : 2), and iodide ions can dissolve the CuI layer. We also how that by coating a layer of copper(II) acetate and utilizing the known Cu(II)/Cu(I) redox chemistry with iodide ions, we can preserve CuI in the presence of halide salts and solvents. [ABSTRACT FROM AUTHOR]

A copper iodide promoted cyclization for the synthesis of isoxazolyl imidazo[1,2‐b]isoxazoles 3 in a one‐pot procedure has been investigated by interaction of 3‐aminoisoxazole 1 with nitrostyrylisoxazoles 2 under aerial oxidation condition. The newly synthesized compounds 3a–l were screened for their in vitro antimicrobial and anti‐inflammatory activities. [ABSTRACT FROM AUTHOR]

Metal halide perovskite scintillators encounter unprecedented opportunities in indirect ionizing radiation detection due to their high quantum yields. However, the long scintillation lifetime of microseconds upon irradiation, known as the afterglow phenomenon, obviously limits their fast development. Here, a new type of hybrid X‐ray detector wafer combining direct methylamine lead iodide (MAPbI3) semiconductor and indirect zero‐dimensional cesium copper iodide (Cs3Cu2I5) scintillator through low‐cost fast tableting processes is reported. Due to the fast energy transfer from Cs3Cu2I5 to MAPbI3, the device response time to X‐rays is dramatically reduced by nearly 30 times to 36.6 ns, which enables fast X‐ray detection capability by a large area detector arrays within 1 s. Moreover, Cs3Cu2I5 exists at the grain boundaries of MAPbI3 crystals, and blocks the paths of mobile ions of perovskite, leading to the lowest detectable dose rate of hybrid X‐ray detector is thus reduced by 1.5 times compared with control MAPbI3 direct‐type semiconductor, and 10 times compared with the Cs3Cu2I5 indirect‐type scintillator. The direct/indirect hybrid wafer also exhibits improved operation stability at ambient conditions without any encapsulation. This new kind of hybrid X‐ray detectors provides strong competitiveness by combining the advantages of both direct perovskite semiconductors and indirect perovskite scintillators for next‐generation products. [ABSTRACT FROM AUTHOR]

Tetranuclear copper‐iodide cluster consisting of a {Cu4I4} cubane and diphenylphosphine ligand has been found as a highly stable precursor for further post‐functionalization through hydrophosphination reaction. UV irradiation of the cluster in the presence of various alkenes allows direct functionalization of the latter, giving access to a wide range of copper cubane complexes, a source of molecular diversity for luminescent materials. Such a strategy provided access to the first example of water‐soluble luminescent cubane copper iodide. [ABSTRACT FROM AUTHOR]

Lead‐free ternary copper iodide perovskite analogues demonstrate great potential in photodetector, due to their nontoxity and excellent photophysical properties. However, the fast carrier recombination limits the photoelectric conversion efficiency. Herein, a room‐temperature growth strategy with the selected raw ratio is adopted to enhance carrier dynamics. The optimized‐grown CsCu2I3 single crystal exhibits longer carrier lifetime of 157 ns, and its switch ratio and response time are enhanced by 20 000% and 600% compared with those of stoichiometric‐grown single crystal, respectively. Furthermore, space‐confined method is introduced to prepare ultralong single‐crystalline CsCu2I3 microbelt, with the aspect ratio up to 600. The sensitivity and self‐powered performance of the UV photodetector are improved through constructing heterojunction with p‐CuI and asymmetric electrodes. The enhanced performance is ascribed to superior type‐II band alignment between CsCu2I3 and CuI, which effectively promotes the separation of photogenerated carriers. This work not only provides an efficient way to boost the photoresponse in low‐dimensional metal halide perovskite analogue, but also displays 1D anisotropic growth for potential application in large‐area vapor‐assisted patterned devices. [ABSTRACT FROM AUTHOR]

The C−N functionalization of thiazole appendant aryl halides using copper mediated transformation has the potential as a strategy for late‐stage Goldberg coupling of carboxamide and heteroaryl halide. The C−N coupling of thiazole scaffold in the presence of copper is highly challenging. The current work presents the C−N coupling of various amides with thiazole derivatives that afforded variety of amide products. The 4‐(4‐bromo‐phenyl)‐2‐methylthiazole, 4‐(4‐bromophenyl)‐2‐pyridiythiazole and 4‐(3‐bromophenyl)‐2‐methylthiazole reacted with aliphatic, aromatic and cyclic amides smoothly in the presence of stoichiometric amount of copper iodide and N,N'‐DMEDA resulting in C−N bond formation in high yields. The reaction optimization attest to the requirement of stoichiometric amount of copper for the thiazolyl aryl bromide. While the corresponding oxazole can easily undergo the amide coupling employing only catalytic amount of copper. [ABSTRACT FROM AUTHOR]

A hierarchical layered architecture in thermoelectric materials works as an ad hoc methodology for strengthening the unique inherent properties. Herein, an excellent thermoelectric behavior in novel 2D copper iodide nanoflakes is demonstrated by compositing with Ti3C2 MXene nanoinclusions. The interlaced architecture of the CuI/Ti3C2 composite lifts the electrical conductivity over two orders by efficient charge transport mechanisms. The thermal conductivity of CuI/Ti3C2 composite is reduced by drastic suppression of mid‐ and high‐frequency phonons by interfacial energy barrier scattering. The structural engineering approach yields a massive power factor of 225 μW m−1 K−2 and a figure of merit value of 0.48 in CuI/5 vol% Ti3C2 composite. A straightforward approach of tuning the figure of merit in Earth‐abundant, nontoxic thermoelectric materials to develop future sustainable energy sources is established. [ABSTRACT FROM AUTHOR]

Broadband white‐light emissions from low‐dimensional organic metal halides have received great attention for applications in energy‐efficient lighting and displays. However, the simultaneous realization of excellent color rendering indexes (CRIs) and high photoluminescence quantum efficiencies (PLQEs) in single‐component white‐light emitters remains a great challenge. Here, a unique 0D organic copper iodide (TPA)CuI2 (TPA = tetrapropylammonium) is developed, in which the edge‐sharing double trigonal planar [Cu2I4]2− dimers are surrounded by the organic cations TPA+, forming core/shell structures at the molecular level. These organic copper iodide single crystals exhibit a dual‐band white‐light emission covering the entire visible spectrum with a high PLQE of 84.4% and an excellent CRI of 91.3. In addition, (TPA)CuI2 nanocrystals are successfully synthesized and exhibit optical properties similar to those of the single‐crystal counterparts. Detailed photophysical studies reveal that the dual‐band emission originates from two self‐trapped emitting states in [Cu2I4]2− dimers, whose populations are strongly dependent on the temperature. The promising applications of (TPA)CuI2 as efficient and high CRI phosphors are demonstrated by a white‐light light‐emitting diode with a Commission Internationale de l'Eclairage coordinate of (0.31, 0.33). [ABSTRACT FROM AUTHOR]

Herein, we report a feasible molecular design of the binuclear clusters featuring the n‐p‐n heterojunction of biligand‐sandwiched inorganic units, which can be used as the effective charge trapper in ambipolar transistor memories with the large memory windows and the energy‐saving operation. We found that the hole confinement on the p‐type inorganic units is enhanced by spatial electronic anisotropy provided by the peripheral n‐type organic phosphine ligands. The steric hindrance of the coordination sites, the insulating effect of the carbon‐phosphorous single bonds and the parallel dual‐ligand coordination mode jointly elongate the interunit distances to nanometer scale and restrain the intramolecular electronic communications, leading to the tunable and reliable charge trapping. Our results show that the spatial effect is crucial to further amplifying the electronic differences between organic and inorganic units for function enhancement. [ABSTRACT FROM AUTHOR]

Herein, we report a feasible molecular design of the binuclear clusters featuring the n‐p‐n heterojunction of biligand‐sandwiched inorganic units, which can be used as the effective charge trapper in ambipolar transistor memories with the large memory windows and the energy‐saving operation. We found that the hole confinement on the p‐type inorganic units is enhanced by spatial electronic anisotropy provided by the peripheral n‐type organic phosphine ligands. The steric hindrance of the coordination sites, the insulating effect of the carbon‐phosphorous single bonds and the parallel dual‐ligand coordination mode jointly elongate the interunit distances to nanometer scale and restrain the intramolecular electronic communications, leading to the tunable and reliable charge trapping. Our results show that the spatial effect is crucial to further amplifying the electronic differences between organic and inorganic units for function enhancement. [ABSTRACT FROM AUTHOR]

At room temperature (RT), the weak and strong cluster‐centered luminescence of silver and copper iodide clusters, respectively, has been widely reported. Though the central metal ions show same d10 electrons and similar coordination mode, the mechanism of their distinct emission properties is still unclear, which restricts further applications. In this work, it is found that different photoluminescence quantum yields (PLQYs) are caused by various collision energy transfers between the metal ions in clusters, like a kind of aggregation‐caused quenching mechanism. Concretely, isostructural coordination polymers (CPs) of Ag(I) and Cu(I) iodide clusters are synthesized. The Ag(I)‐CP shows no luminescence at RT while the PLQY of Cu(I)‐CP boosts to 89%, in which short radius and weak collision between metal ions are found. Moreover, shorter Cu(I)‐Cu(I) and longer Ag(I)‐Ag(I) distances are realized in the similar structure and they display prospective luminescence, which proves the collisional quenching mechanism. Inspired of the above, the heterometallic materials with high sensitivities and wide sensing windows to temperature detection are obtained through tuning the metal content, and they are also fabricated into detecting sequences, which satisfies the wide‐range temperature sensing. This work proposes an efficient strategy to improve RT photoluminescence and broaden temperature sensing windows. [ABSTRACT FROM AUTHOR]

Graphdiyne (g−CnH2n‐2), a novel two‐dimension carbon allotrope material composed of a sp‐ and sp2‐hybrid carbon network, has been widely explored since it was synthesized for the first time by Li's group in 2010. A series distinct and excellent properties bestow graphdiyne excellent performance in many fields. Here, an innovative progress for preparing graphdiyne by using Cu+ contained material as catalyst is reported and the composite CuI‐GD is coupled with flower‐like NiAl‐LDH to produce H2 from photocatalytic water splitting. The results of FTIR and Raman spectroscopy together reveal that graphdiyne nanosheets are synthesized successfully by employing a cross‐coupling method. Photocatalytic hydrogen evolution performance shows that the hydrogen production activity of CuI‐GD/NiAl‐LDH has a 15‐ and 216‐fold enhancement compared with CuI‐GD and NiAl‐LDH, respectively. A series of characterizations are carried out to expound the underlying reasons in the enhancement of the photocatalytic hydrogen production performance of CuI‐GD/NiAl‐LDH. Meanwhile, a possible mechanism for the photocatalytic hydrogen evolution process was proposed to understand the interaction among these materials. [ABSTRACT FROM AUTHOR]

Developing transparent p‐type semiconductors and conductors has attracted significant interest in both academia and industry because metal oxides only show efficient n‐type characteristics at room temperature. Among the different candidates, copper iodide (CuI) is one of the most promising p‐type materials because of its widely adjustable conductivity from transparent electrodes to semiconducting layers in transistors. CuI can form thin films with high transparency in the visible light region using various low‐temperature deposition techniques. This progress report aims to provide a basic understanding of CuI‐based materials and recent progress in the development of various devices. The first section provides a brief introduction to CuI with respect to electronic structure, defect states, charge transport physics, and overviews the CuI film deposition methods. The material design concepts through doping/alloying approaches to adjust the optoelectrical properties are also discussed in the first section. The following section presents recent advances in state‐of‐the‐art CuI‐based devices, including transparent electrodes, thermoelectric devices, p–n diodes, p‐channel transistors, light emitting diodes, and solar cells. In conclusion, current challenges and perspective opportunities are highlighted. [ABSTRACT FROM AUTHOR]

An efficient and retrievable copper(I) catalyst was synthesized by immobilizing of copper iodide on 3‐thionicotinyl‐urea‐modified magnetic nanoparticles and characterized using a variety of analysis techniques. The catalytic activity of these nanoparticles was investigated in the one‐pot three‐component reaction of aryl halides, sodium azide, and terminal alkynes using choline chloride/PEG deep eutectic mixture as a green and recoverable solvent. The PEGylated deep eutectic solvent (DES), due to its favorable polarity and solubility, can make an effective association of polar and non‐polar reactants during the reaction, thereby accelerating the catalysis process. An array of 1‐aryl 1,2,3‐triazoles were obtained in good to excellent yields. The catalyst system can be readily recovered and reused at least five times with no appreciable loss of its activity. [ABSTRACT FROM AUTHOR]

Cuprous halides, best described as (CuX)n (X = Cl−, Br−, and I−) in their solid state, catalyse selective aerobic oxidation of alcohols with the assistance of both NMI (N‐methylimidazole) and TEMPO (2,2,6,6‐tetramethylpiperidine‐1‐oxyl), and the iodide generally demonstrates the highest activity, for example, in the oxidation of 1‐octanol at ambient temperature under 24 h' reaction. However, in the aerobic oxidation of benzylic alcohols, the chloride showed superiority to the iodide in that the aerobic oxidation was quantitatively completed within 3 h at ambient temperature whereas the iodide showed only about half the activity of the chloride analogue. By probing the system using electrochemistry, electric conductivity, and 1H NMR titration, it was revealed that the surprising anomaly was due to the difference in the rate of forming active species, [Cu (NMI)2X(MeCN)], from the polymeric solid in a two‐stage process. Substrates expansion of 11 benzylic alcohols indicated that CuCl/NMI/TEMPO system demonstrated quantitative conversion of benzylic alcohols into corresponding aldehydes within 3 h and showed great tolerance to the substituents on the phenyl ring of the substrates. Furthermore, electron‐withdrawing substituent was beneficial to the oxidation and could offset the steric effect at orthro‐substituent. Such a behaviour suggested that in the catalysis, increasing the acidity of the hydroxyl group (OH) of the substrates could ease the oxidation, which implied that the deprotonation via an internal pathway might be one of the rate‐determining steps. Our results also showed that the anion halide participated actively in the catalysis by coordinating to Cu(I) in the active species. [ABSTRACT FROM AUTHOR]

Benzothiazole is one of the most important heterocyclic scaffolds existing in both natural and synthetic compounds. This prominent ring is of undoubted interest due to its broad range of therapeutic benefits as well as chemical reactivity in organic reactions. Therefore, we developed a convenient, rapid and efficient methodology for the ring closure reaction of thioureas to form 2-aminobenzothiazole derivatives. We optimized the reaction conditions by trying various catalysts and oxidants. Copper iodide/oxone catalysis provided the best conditions for the preparation of benzothiazoles. The regioselectivity observed in the ring closure reaction of the naphthyl thiourea derivative was investigated and the obtained experimental results were supported by theoretical calculations. In vitro antimicrobial effects of the compounds were tested against various bacterial and fungal strains. Finally, molecular docking studies were carried out to rationalize the achieved biological results and suggest molecular modifications to design new benzothiazole derivatives. [ABSTRACT FROM AUTHOR]

This paper demonstrates a selective, mild approach to Ullmann amination of aryl halides to synthesize N‐alkylated derivatives of ϵ‐caprolactam. The synthetic route involves an in‐situ ring‐opening of 1,8‐diazabicyclo[5.4.0]undec‐8‐ene (DBU) followed by concurrent arylation with aryl halides in the presence of copper iodide as a catalyst under ligand‐free conditions. This method provides a new entry to a wide variety of ϵ‐caprolactam derivatives in good to excellent yields in a single synthetic sequence. Similarly, other bicyclic amidines such as 1, 5‐diazabicyclo‐[4.3.0]non‐5‐ene (DBN), and 1,5,7 triazabicyclo[4.4.0] dec‐5‐ene (TBD) also showed good to very high reactivity. Azepan‐2‐one, or Caprolactam, is an important synthon in polymer chemistry and has a global demand as it is employed to make Nylon 6 filament, fiber, and plastics.[1] The global caprolactam market size is expected to expand for the growing textile industry with rising demand for plastics in the construction of automotive, electrical, and electronic sectors. Additionally, technological advancements aimed at improving the cost‐effective manufacturing process of caprolactam, to minimize the release of hazardous waste into the environment is of vital necessity. Derivatives of ϵ‐caprolactam are of interest for the production of modified nylons[2] and nanogels.[3] Several Azepinones and their analogs play an important role in medicinal chemistry,[4] used in the synthesis of pharmaceutical drugs including Benazepril,[5] Telcagepant,[6] and Ivabradine.[7] [ABSTRACT FROM AUTHOR]

Optical absorption and emission spectra are the important quantifiable properties for CuI as a promising optoelectronic material. Previous research on the sputter deposition of CuI focuses on room‐temperature growth. Herein, the effect of growth temperature on the selected optical features of sputtered CuI thin films is investigated. An enhanced visible light transparency and a steeper absorption edge are achieved for CuI thin films by optimizing the growth temperature. The PL intensity ratio of free exciton to defect‐related emission increases with increasing substrate temperature. These results suggest a strategy of growth temperature optimization for the enhanced absorption and emission of CuI for advanced optoelectronic applications. [ABSTRACT FROM AUTHOR]

Studies of environmentally benign catalytic methods are of great value in modern chemical synthesis, especially the chemo‐selective construction of chemical bonds under green conditions. This work elucidates such preferential synthesis of C−N bond over C−O bond via selective N‐arylation of 3‐aminophenols using 1,3‐bis‐[2‐hydroxyphenyl] imidazolium chloride (IHPHCl) and copper iodide as catalyst (1 mol %) in aqueous medium. Presence of chelating group (−OH) on IHPHCl enhances N‐selectivity. Overall this is a simple and green method for selective N‐arylation of 3‐aminophenols with good substrate scope and yields (60–88 %). GC‐MS, HRMS and other spectroscopic techniques were utilised in detailing the kinetics and mechanistic aspects. [ABSTRACT FROM AUTHOR]

In the present work, novel 5‐((1‐benzyl‐1,2,3‐triazol‐4‐yl)methoxybenzylidene)‐2‐(arylamino)thiazol‐4‐one thiazolone incorporated triazole derivatives have been designed as tyrosinase inhibitors. The compounds were synthesized through click reaction in good yield. Moreover, the antityrosinas activity of the synthesized derivatives was evaluated. In the search for establishing a click copper‐catalyzed azide/alkyne cycloaddition (CuAAC) reaction under strict conditions, in terms of a novel air‐stable, a recyclable and efficient magnetic catalyst was planned for new triazole derivatives as a well‐organized copper iodide supported on the functionalized Fe3O4@SiO2 core‐shell (CuI/Fe3O4@SiO2(TMS‐EDTA) nanoparticles). The engineered nanocatalyst synthesized for the first time and characterized by different methods, including FT‐IR spectroscopy, XRD, FESEM, EDX, TEM, TGA, and BET analysis. The excellent catalytic performance in ethanol with high surface area (351.7 m2g−1) and short reaction time for diverse functional groups (120–200 min), no use of toxic solvents, reusability of the catalyst, and using eco‐friendly conditions are the advantageous of this work. Moreover,the nanocatalyst can be used at least five times without any significant decrease in the yield of the reaction. The thiazolidine‐triazole derivatives 9a, 9c, 9e, and 9 g showed promising tyrosinase inhibitory activity with IC50 values in the range of 5.90–9.81 μM. The compounds were found to be considerably more potent tyrosinase inhibitors than the reference inhibitor kojic acid (IC50 = 18.36 μM). [ABSTRACT FROM AUTHOR]

Semiconducting cuprous iodide (CuI) nanocrystals have been synthesized by the one‐pot sonochemical method at room temperature. The synthesis was performed in aqueous medium using ascorbic acid, polyvinyl pyrrolidone, p‐toluene sulfonic acid and docusate sodium as surfactants. X‐ray diffraction (XRD) study of resulting material reveals the crystalline nature, cubic zinc blende lattice structure and γ phase of CuI nanocrystals. Scherrer method, Williamson‐Hall plot and Size‐Strain plot method have been used to investigate the particle size and intrinsic strain values from the XRD analysis. Field emission scanning electron microscopy (FESEM) revealed the morphology and different shapes (truncated tetrahedron, irregular, hexagonal & clustered) of CuI nanocrystals synthesized using different surfactants. In the PL spectrum of γ‐CuI nanoparticles strong near band‐edge emission was observed at about 423 nm. A slight red‐shift in near band edge emission was observed due to the presence of surfactants. Enhanced electrical conductivity values (1.96 S/cm–9.19 S/cm) were obtained due to the presence of surfactants for γ‐CuI nanocrystals. These properties of CuI nanocrystals makes them a suitable material for the design and development of optoelectronic devices. [ABSTRACT FROM AUTHOR]

The design of metal–organic frameworks (MOFs) that incorporate more than one metal cluster constituent is a challenging task. Conventional one‐pot reaction protocols require judicious selection of ligand and metal ion precursors, yet remain unpredictable. Stable, preformed nanoclusters, with ligand shells that can undergo additional coordination‐driven reactions, provide a platform for assembling multi‐cluster solids with precision. Herein, a discrete Co6S8(PTA)6 (PTA=1,3,5‐triaza‐7‐phosphaadamantane) superatomic‐metalloligand is assembled into a three‐dimensional (3D) coordination polymer comprising Cu4I4 secondary building units (SBUs). The resulting heterobimetallic framework (1) contains two distinct cluster constituents and bifunctional PTA linkers. Solid‐state diffuse reflectance studies reveal that 1 is an optical semiconductor with a band‐gap of 1.59 eV. Framework‐modified electrodes exhibit reversible redox behavior in the solid state arising from the Co6S8 superatoms, which remain intact during framework synthesis. [ABSTRACT FROM AUTHOR]

Recently, Jun et al. (Adv. Mater.2018, 30, 1706573) reported Sn‐doped amorphous phases of CuI (a‐CuI) as a new class of transparent p‐type semiconductors. It is surprising that high mobilities are found despite amorphous structures tend to localize carriers, particularly the directional p orbitals of anions. To reveal the microscopic origin of the new p‐type amorphous semiconductors, density functional theory calculations are performed, and structural and electrical properties of a‐CuI are investigated. Amorphous models from melt‐quench simulations consist of structural motifs that resemble local orders in crystalline polymorphs of CuI. Despite the absence of translational symmetry, states at valence band maximum (VBM) are substantially extended in linear ways due to the hybridization between I‐5p states, explaining the high hole mobilities in the experiment. Sn‐doped a‐CuI is also investigated and it is found that Sn atoms stabilize the amorphous structure without disturbing the hole transport. Furthermore, results on nonstoichiometric models show that Cu‐deficiency increases the hole concentration in a‐CuI and also enhances the delocalization of VBM states, which is consistent with the experimental observation that the hole mobility increases with doping concentrations. Herein, the origin of hole conduction in amorphous CuI is enlightened, which is believed to contribute in the development of high‐performance p‐type amorphous materials. [ABSTRACT FROM AUTHOR]

New triazole‐imidazole and tetrazole‐imidazole hybrids were obtained using 2,4,5‐triaryl‐1‐(4‐aminophenyl) imidazoles by copper‐catalyzedazide‐alkyne cycloaddition (CuAAC) and Ugi‐azidefour‐component(UA‐4CRs) process. The synthesis of triazole hybrids was performed in the presence of new copper‐incorporated white sandstone nanocatalyst, which was fully characterized by different methods. The construction of newly prepared hybrids was confirmed by spectroscopic techniques. Some of these compounds were evaluated for their anti‐cancer properties against MCF‐7 cancer cell lines. The absorption and emission parameters of the triazole‐ and tetrazole‐substituted imidazoles were also investigated and compared with each other. [ABSTRACT FROM AUTHOR]

Renewable mineral derived nanocatalysts are of special interest to accomplish green and sustainable goals with unique advantages over homogeneous catalysts such as recyclability, robustness, superior activity and minimum waste generation. Here, we synthesized reduced graphene oxide supported copper iodide (RGO@CuI) nanocomposites from renewable malachite mineral derived RGO@CuO precursor by treatment with NH2OH and KI in water. The characterization results reveal the role of RGO sheets as capping agent and supporting material for CuO seeds which control the diffusion of iodide, NH2OH reagents and stabilizes the generated CuI prism morphologies. The RGO@CuI‐20 nanocatalyst is robust to produce wide range of N‐heterocycles such as 5‐diarylamino benzimidazole and spiropyrroline via aerobic and anaerobic single electron transfer (SET) reactions, respectively. The nanocatalysis study delineates two distinct mechanistic pathways for aerobic and anaerobic SET reactions. The present method offers the advantages of utilizing a renewable copper precursor for catalyst preparation, catalyst recyclability over five times, excellent product yields and green reaction conditions with minimum waste (Low E‐factor). [ABSTRACT FROM AUTHOR]

As organic solar cells (OSCs) and perovskite solar cells (PVSCs) move closer to commercialization, further efforts toward optimizing both cell efficiency and stability are needed. As interfaces strongly affect device performance and degradation processes, interfacial engineering by employing various materials as hole transport layers (HTLs) and electron transport layers (ETLs) has been a very active field of research in OSCs and PVSCs. Among them, inorganic materials exhibit significant advantages in promoting device performance due to their excellent charge transporting properties and intrinsic thermal and chemical robustness. In this review, an extensive overview is provided of inorganic semiconductors such as copper‐based ones with emphasis on copper iodide and copper thiocyanate, transition metal chalcogenides, nitrides and carbides as well as hybrid materials based on these inorganic compounds that have been recently employed as HTLs and ETLs in OSCs and PVSCs. Following a short discussion of the main optoelectronic and physical properties that interfacial materials used as HTLs and ETLs should possess, the functionalities of the aforementioned materials as interfacial, charge transport, layers in OSCs and PVSCs are discussed in depth. It is concluded by providing guidelines for further developments that could significantly extend the implementation of these materials in solar cells. [ABSTRACT FROM AUTHOR]

A facile iodine‐mediated unprecedented C–C cleavage by employing CuI has been established towards the synthesis of quinazolin‐4(3H)‐ones and benzo[4,5]imidazo[1,2‐c]quinazolines. This protocol involves peroxide free synthetic approach for the stable C–C bond cleavage followed by oxidative annulation to develop a library of fused N‐heterocyclic molecules. [ABSTRACT FROM AUTHOR]

Graphdiyne (GD), a novel two‐dimension carbon hybrid material, due to its unique and excellent properties, has been widely concerned since this innovative material was successfully synthesized by Prof. Yuliang Li in 2010. Traditionally, its synthesis method is growing graphdiyne on copper foils or foam copper as a base catalytic material to deliver copper ions (Cu2+) under pyridine conditions. Here, an innovative progress for graphdiyne preparation approach of using Cu+ ion as a catalytic material is reported and its application in extending to the photocatalytic water‐splitting to produce hydrogen in situ as well. In detail, by means of cuprous iodide used as a catalyst‐carrier to grow a graphdiyne in a pyridine solution of monomeric hexynylbenzene and such CuI‐graphdiyne composite catalyst is directly applied to photocatalytic hydrogen production in situ. Meanwhile, the hydrogen production of GD and CuI are 29.42 μmol/5 h and 156.49 μmol/5 h, respectively. In particular, the composite catalyst GD‐CuI exhibits an optimum photo‐catalytic hydrogen production activity (465.95 μmol/5 h) which is 15.8 times and 3.0 times that of pure GD and CuI respectively. This rational design, one‐step construction of GD‐CuI, successfully enhances photo‐catalytic hydrogen evolution activity. The deeper characterization study results such as TEM, SEM, XPS, XRD, UV‐vis DRS, Transient photocurrent and FT‐IR etc. have been well researched and the results of which are in good agreement with each other. [ABSTRACT FROM AUTHOR]

An efficient, simple and economic Morita‐Baylis‐Hillman approach for construction of 3‐hydroxy‐3‐substituted‐2‐oxindole was proceeded smoothly from isatin derivatives and methyl acrylate/acrylonitrile using mild catalytic conditions. It was demonstrated that proper selection of catalyst and reaction medium would differentiate the feasibility of reaction and yield of the final product. Reaction condition was explored the novel combination of Copper Iodide (CuI) and 1,8‐Diazabicyclo [5.4.0] undec‐7‐ene (DBU) in the presence of dichloromethane (DCM) as the medium. This strategy provides a facile access to various derivatives with good to excellent yields in short span of time. The resulting derivatives can serve as a valuable synthetic building block for pharmaceuticals and natural products. [ABSTRACT FROM AUTHOR]