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The current work aims to generate multifunctional MOFs by incorporating a well-known inorganic motif, a trinuclear Cu-pyrazolate [Cu3(μ3-OH)(μ-Pyz)3] (T-CuP) unit, as a node of the network. Accordingly, we report herein the synthesis and properties of five new compounds using five V-shaped dicarboxylic acids as auxiliary ligands. The structural features are consistent with the theme of grafting T-CuP units as nodal points of architectures whose chassis are primarily made of bent acids. V-shaped acids also induce a helical nature inside resulting frameworks. Beside their structural and physical features, T-CuP unit-based MOFs also vindicate our thematic approach of the trinuclear Cu-pyrazolate unit imparting specific physicochemical properties, such as magnetic, electrical, and catalytic properties, to resultant MOFs. The MOFs show excellent catalytic properties in reducing 4-nitrophenol, which could be attributed to the porous nature of the network along with the presence of metal centres with unsaturated coordination within the T-CuP unit. Furthermore, efficient photocatalytic degradation of harmful organic dyes confirms their importance for environmental remediation. The presence of a T-CuP unit and various functional groups also make some of the MOFs suitable candidates for electrical applications, which is indeed manifested in encouraging proton conductivity. Finally, the potential of current MOFs, fitted with a magnetically important trinuclear Cu-pyrazolate motif, as magnetic materials has also been thoroughly investigated. [ABSTRACT FROM AUTHOR]

Besides iron, ironically neodymium (Nd) is the most ubiquitously used metal for magnetic purposes, even among the lanthanides, when it comes to the field of molecular magnetism, yet it ranks among the least studied metals. However, strong apathy towards this magnetic lanthanide means that vital information will be missed, which is required for the advancement of the subject. Herein, we have successfully demonstrated the usefulness of a hexanuclear neodymium complex as a magnetic material, and also in electronic device fabrication. A {Nd III6 } cage with an aesthetically pleasing butterfly topology was synthesized using a rather non-conventional N-rich pyridyl-pyrazolyl based ligand. The cage shows single molecule magnet (SMM) properties, with an effective energy barrier, Ueff, value of 3.4 K and relaxation time, τ0, of 3.1 × 10−4 s, originating from an unusual occurrence of metal centres with different coordination environments. Furthermore, magnetic studies reveal significant cyrogenic magnetic cooling, with a magnetic entropy change of 8.28 J kg−1 K−1 at 5 T and 3 K. To the best of our knowledge, the titular compound is the only example of a Nd-complex that exhibits concomitant magnetocaloric effect (MCE) and SMM properties. Complete active space self-consistent field (CASSCF) calculations were carried out to shed light on the origin of the magnetic anisotropy and magnetic relaxation of the compound. The same uniqueness is also true for the first electronic investigation carried out on the Nd complex. The maiden electronic device fabricated using the Nd complex shows an interesting intertwining of electronic and optical features, which contribute towards its improved photosensitized optoelectronic data. [ABSTRACT FROM AUTHOR]

Abstract: In this article, we report four pyridyl‐pyrazolyl based polynuclear cluster complexes with Ln8 {Ln=[GdIII8(μ3‐OH)4(L1)4(DEA)4Cl4](DMF)2(MeOH)(1), [HoIII8(μ3‐OH)4(L1)4(DEA)4Cl4](2), [ErIII8(μ3‐OH)4(L1)4(DEA)4Cl4](DMF)(MeOH)(H2O)(3), [YbIII8(μ3‐OH)4(L1)4(DEA)4Cl4](DMF)(MeOH)(4) [DEA = Diethanolamine] cores. The impetus for this study was to explore the magnetic behaviour of lanthanide ions which are often ignored or overlooked. X‐ray crystal analysis show that these complexes are isostructural and exhibit an interesting butterfly like topology. The semi‐rigidity and asymmetric nature of the ligand led to different coordination environment around the metal centres. The lanthanide ions adopt two types of geometry, a bicapped trigonal prism and a distorted square antiprismatic geometry around the metal center. Such dissimilar coordination environments around the lanthanide centre can have profound effects on their magnetic behaviour. Indeed, the magnetic measurements revealed significant magnetocaloric effect for octanuclear gadolinium complex 1 with magnetic entropy change (−ΔSm ) of 31.4 J kg−1 K−1 for ΔH = 9 T at T = 3 K whereas Er analogue complex 3 displayed SMM behavior. [ABSTRACT FROM AUTHOR]

Employment of two different pyridyl-pyrazolyl-based ligands afforded three octanuclear lanthanide(III) (Ln = Dy, Tb) cage compounds and one hexanuclear neodymium(III) coordination cage, exhibiting versatile molecular architectures including a butterfly core. Relatively less common semirigid pyridyl-pyrazolyl-based asymmetric ligand systems show an interesting trend of forming polynuclear lanthanide cage complexes with different coordination environments around the metal centers. It is noteworthy here that construction of lanthanide complex itself is a challenging task in a ligand system as soft N-donor rich as pyridyl-pyrazol. We report herein some lanthanide complexes using ligand containing only one or two O-donors compare to five N-coordinating sites. The resultant multinuclear lanthanide complexes show interesting magnetic and spectroscopic features originating from different spatial arrangements of the metal ions. Alternating current (ac) susceptibility measurements of the two dysprosium complexes display frequency- and temperature-dependent out-of-phase signals in zero and 0.5 T direct current field, a typical characteristic feature of single-molecule magnet (SMM) behavior, indicating different energy reversal barriers due to different molecular topologies. Another aspect of this work is the occurrence of the not-so-common SMM behavior of the terbium complex, further confirmed by ac susceptibility measurement. [ABSTRACT FROM AUTHOR]

A novel ligand N,N'-di-(3-(pyridin-2-yl)-1H-pyrazole-5-carbohydrazide) naphthalene 1,4,5,8-tetracarboxylic acid bisimide (PPNB) and its nickel (II) complex (Ni-PPNB) were synthesized and systematically characterized. Both the molecules show higher sensitization activity on the TiO2 semiconducting system. These composites have interesting photophysical properties as they enable photocatalytic hydrogen production from water with a sacrificial electron donor (SED) using visible light, while neither component alone is able to do so. The photocatalysts have shown long term stability and a maximum turnover number (TON) of 7866 based on Ni-PPNB was obtained after 6 h of irradiation at a catalyst concentration of 2.5 × 10-5 mol g-1. [ABSTRACT FROM AUTHOR]

The present work reports the constructionand self-assembly studiesof molecular helix and polyhedral coordination cages using a pyridine-pyrazolebased asymmetric ligand. Employment of different metals has resultedin different architectures ranging from a one-dimensional helicalpolymer, [2 × 2] grid to a pentanuclear cage. For all the structures,hydrogen bonding and π–π stacking were found tobe instrumental in bringing additional stability to the polymericnetworks. Furthermore, chirality and magnetic properties of cobaltand copper complexes have also been investigated. [ABSTRACT FROM AUTHOR]

The current work aims to generate multifunctional MOFs by incorporating a well-known inorganic motif, a trinuclear Cu-pyrazolate [Cu 3 (μ 3 -OH)(μ-Pyz) 3 ] (T-CuP) unit, as a node of the network. Accordingly, we report herein the synthesis and properties of five new compounds using five V-shaped dicarboxylic acids as auxiliary ligands. The structural features are consistent with the theme of grafting T-CuP units as nodal points of architectures whose chassis are primarily made of bent acids. V-shaped acids also induce a helical nature inside resulting frameworks. Beside their structural and physical features, T-CuP unit-based MOFs also vindicate our thematic approach of the trinuclear Cu-pyrazolate unit imparting specific physicochemical properties, such as magnetic, electrical, and catalytic properties, to resultant MOFs. The MOFs show excellent catalytic properties in reducing 4-nitrophenol, which could be attributed to the porous nature of the network along with the presence of metal centres with unsaturated coordination within the T-CuP unit. Furthermore, efficient photocatalytic degradation of harmful organic dyes confirms their importance for environmental remediation. The presence of a T-CuP unit and various functional groups also make some of the MOFs suitable candidates for electrical applications, which is indeed manifested in encouraging proton conductivity. Finally, the potential of current MOFs, fitted with a magnetically important trinuclear Cu-pyrazolate motif, as magnetic materials has also been thoroughly investigated.

The present work is part of our ongoing quest for developing functional inorganic complexes using unorthodox pyridyl-pyrazolyl-based ligands. Accordingly, we report herein the synthesis, characterization, and luminescence and magnetic properties of four 3d-4f mixed-metal complexes with a general core of Ln 2 Zn 6 (Ln = Dy, Gd, Tb, and Eu). In stark contrast to the popular wisdom of using a compartmental ligand with separate islands of hard and soft coordinating sites for selective coordination, we have vindicated our approach of using a ligand with overcrowded N-coordinating sites that show equal efficiency with both 4f and 3d metals toward multinuclear cage-cluster formation. The encouraging red and green photolumiscent features of noncytotoxic Eu 2 Zn 6 and Tb 2 Zn 6 complexes along with their existence in nanoscale dimension have been exploited with live-cell confocal microscopy imaging of human breast adenocarcinoma (MCF7) cells. The magnetic features of the Dy 2 Zn 6 complex confirm the single-molecule-magnet behavior with befitting frequency- and temperature-dependent out-of-phase signals along with an U eff value of ∼5 K and a relaxation time of 8.52 × 10 -6 s. The Gd 2 Zn 6 complex, on the other hand, shows cryogenic magnetic refrigeration with an entropy change of 11.25 J kg -1 K -1 at a magnetic field of 7 T and at 2 K. Another important aspect of this work reflects the excellent agreement between the experimental results and theoretical calculations. The theoretical studies carried out using the broken-symmetry density functional theory, ORCA suite of programs, and MOLCAS calculations using the complete-active-space self-consistent-field method show an excellent synergism with the experimentally measured magnetic and spectroscopic data.

A novel ligand N,N'-di-(3-(pyridin-2-yl)-1H-pyrazole-5-carbohydrazide) naphthalene 1,4,5,8-tetracarboxylic acid bisimide (PPNB) and its nickel (ii) complex (Ni-PPNB) were synthesized and systematically characterized. Both the molecules show higher sensitization activity on the TiO2 semiconducting system. These composites have interesting photophysical properties as they enable photocatalytic hydrogen production from water with a sacrificial electron donor (SED) using visible light, while neither component alone is able to do so. The photocatalysts have shown long term stability and a maximum turnover number (TON) of 7866 based on Ni-PPNB was obtained after 6 h of irradiation at a catalyst concentration of 2.5 × 10(-5) mol g(-1).

The centrosymmetric binuclear Cu(II) title complex, [Cu(2)(C(8)H(7)O(3))(4)(CH(3)CN)(2)], has a paddle-wheel-type structure [Cu-Cu distance = 2.6433 (3) Å]. Each Cu(II) ion is coordin-ated by four O atoms from two 3-meth-oxy-benzoate ligands and one acetonitrile N atom in a square-pyramidal geometry.