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An efficient synthetic strategy that includes protection–modification–deprotection consequence was successfully developed to obtain novel water-soluble, amphiphilic, surface-active maltodextrin-based glycosilicones.

We devise a high-carrier-mobility hole-transport layer with less hole loss, obtained via doping poly(9-vinylcarbazole) into poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-(4,4′-(N-(4-butylphenyl)))], achieving high external quantum efficiency QLEDs (22.7%).

Photoluminescent lanthanide complexes of Eu

The architecture of transparent contacts is of utmost importance for creation of efficient flexible light-emitting devices (LEDs) and other deformable electronic devices. We successfully combined the newly synthesized transparent and durable silicone rubbers and the semiconductor materials with original fabrication methods to design LEDs and demonstrate their significant flexibility. We developed electrodes based on a composite GaP nanowire-phenylethyl-functionalized silicone rubber membrane, improved with single-walled carbon nanotube films for a hybrid poly(ethylene oxide)-metal-halide perovskite (CsPbBr3) flexible green LED. The proposed approach provides a novel platform for fabrication of flexible hybrid optoelectronic devices.

Polysiloxanes and materials based on them (silicone materials) are of great interest in optoelectronics due to their high flexibility, good film-forming ability, and optical transparency. According to the literature, polysiloxanes are suggested to be very promising in the field of optoelectronics and could be employed in the composition of liquid crystal devices, computer memory drives organic light emitting diodes (OLED), and organic photovoltaic devices, including dye synthesized solar cells (DSSC). Polysiloxanes are also a promising material for novel optoectronic devices, such as LEDs based on arrays of III–V nanowires (NWs). In this review, we analyze the currently existing types of silicone materials and their main properties, which are used in optoelectronic device development.

A family of the C,N-cyclometalated species [Pt(ppy)Cl(PPh3)], [Pt(ppy)Cl(CNCy)], [Pt(ppy)(CNCy)(PPh3)](OTf), and [Pt(ppy)(CNCy)2](BF4) (ppy = 2-phenylpyridinato-C2,N; Cy = cyclohexyl) was generated...

Photoluminescent lanthanide complexes of Eu3+ and Tb3+ as central atoms and N6,N6’-diisopropyl-[2,2′-bipyridine]-6,6′-dicarboxamide as ligand were synthesized. The structure of these complexes was established by single-crystal X-ray diffraction, mass spectrometry, 1H and 13C nuclear magnetic resonance, ultraviolet-visible, infrared spectroscopy, and thermogravimetry. Bipyridinic ligands provide formation of coordinatively saturated complexes of lanthanide ions and strong photoluminescence (PL). The Eu3+- and Tb3+-complexes exhibit PL emission in the red and green regions observed at a 340 nm excitation. The quantum yield for the complexes was revealed to be 36.5 and 12.6% for Tb3+- and Eu3+-complexes, respectively. These lanthanide compounds could be employed as photoluminescent solid-state compounds and as emitting fillers in polymer (for example, polyethylene glycol) photoluminescent materials.

C,N-Chelate deprotonated diaminocarbene platinum(II) complexes were synthesized by coupling coordinated isocyanides and azinyl-substituted ureas. The complexes act as catalysts of α,ω-divinylpolydimethylsiloxane and poly(dimethylsiloxane-co-methylhydrosiloxane) hydrosilylation cross-linking. Silicone rubbers obtained with (aminoisoquinoline)-containing complex 3d exhibit temperature-responsive luminescence. Their emission changes irreversibly when heated from 80–100 °C (green radiation) to 120 °C or more (blue radiation).

The architecture of transparent contacts is of utmost importance for creation of efficient flexible light-emitting devices (LEDs) and other deformable electronic devices. We successfully combined the newly synthesized transparent and durable silicone rubbers and the semiconductor materials with original fabrication methods to design LEDs and demonstrate their significant flexibility. We developed electrodes based on a composite GaP nanowire-phenylethyl-functionalized silicone rubber membrane, improved with single-walled carbon nanotube films for a hybrid poly(ethylene oxide)-metal-halide perovskite (CsPbBr

Rubber materials are the key components of flexible optoelectronic devices, especially for the light-emitting diodes based on arrays of inorganic nanowires (NWs). This paper reports on polydimethylsiloxane-graft-polystyrene (PDMS-St) as a new flexible substrate of GaP NW array structures. The NWs were encapsulated by the newly introduced G-coating method to substitute the inefficient mainstream spin-coating. To further exploit the flexibility and the stretchability of the NW/PDMS-St structures, the ferrocenyl-containing polymethylhydrosiloxane was synthesized and successfully used as an electrode for the NWs. In order to make an alternative highly efficient transparent electrode, a new application of conductive single-walled carbon nanotubes was demonstrated. The novel materials and methods demonstrated unsurpassed mechanical stability of the fabricated flexible electronic devices.

4-Substituted O-benzyl benzamide oximes reacted with 2-iodobenzonitrile in the presence of 0.1 mol % of [Pd2(dba)3], 0.2 mol % of XantPhos, and 1.5 equiv of Cs2CO3 in dioxane under argon to give 2-arylquinazolin-4-amines. The described reaction is a new type of cascade processes, which affords 4-amino-quinazoline derivatives without using highly reactive chlorinating agents.

Acetylacetonate and 4-arylimino-2-pentanonate carbonyl complexes of rhodium(I) [Rh(RC(O)C(R')C(O)R“)(CO)2] (1: R = Me, R' = H, R'' = Me; 2: R = Me, R' = Cl, R'' = Me; 3: R = Me, R' = H, R'' = CO2Me; 4: R = Ph, R' = H, R'' = Me; 5: R = Ph, R' = H, R'' = Ph) and [Rh(MeC(NR''')CHC(O)Me)(CO)2] (6: R''' = Ph; 7: R''' = 2,6-Me2C6H3) were examined as hydrosilylation cross-linking catalysts at RT for the reaction of poly(dimethylsiloxane-co-ethylhydrosiloxane) copolymer with vinyl terminated poly(dimethylsiloxane) or vinyl terminated poly(dimethylsiloxane-co-styrene) copolymer. All complexes allow cross-linking of vinyl- and hydride-containing polysiloxanes and copolymers at RT without inhibitor addition. Complexes 1–7 possess catalytic activity comparable to the industrially used complex of Pt0 and divinyltetramethyldisiloxane (Karstedt’s catalyst). 1 is the most active among the studied rhodium complexes at 1.0 × 10−4 mol⋅L−1 and 1.0 × 10−5 mol⋅L−1. Silicone rubbers obtained with the rhodium catalysts compared to Karstedt’s catalyst possess no visible defects (bubbles or cracks), and differed by improved elastic properties (the elongation at break increased from 160 to 255%) The activity and improved silicone rubber properties using 1 renders it one of the suitable alternatives to Karstedt’s catalyst.

The laser induced curing of acryloxy terminated ethyleneoxide dimethylsiloxane-ethyleneoxide ABA block copolymer (PDMS-AO) and (3-glycidoxypropyl)trimethoxysilane (GPTMS) was carried out with 2-hydroxy-2-methylpropiophenone as radical photoinitiator and p-(octyloxyphenyl)phenyliodonium hexafluoroantimonate as cationic photoinitiator, respectively. The cross-linking mechanisms for both mixtures were determined through monitoring of photocuring by SSNMR, FTIR and Raman spectroscopies. The obtained silicone rubbers were tested by swelling measurements and thermogravimetric analysis. In comparison with PDMS-AO, cross-linked GPTMS had slightly more cross-linking density (by approximately 20% more). The cross-linked GPTMS was more thermally stable in air than cured PDMS-AO (by c.a. 190° C) due to both mechanisms: epoxy polymerization and Si–O–Si formation. The possibility of laser printing with defined framework for PDMS-AO was successfully demonstrated that allows obtaining laser printed polymer objects.

Flexible optoelectronic structures are required in a wide range of applications. Large scale modified silicone-embedded n-GaP nanowire arrays of a record 6 µm thin membranes were studied. A homogeneous silicone encapsulation was enabled by G-coating using a heavy-load centrifuge. The synthesized graft-copolymers of polydimethylsiloxane (PDMS) and polystyrene demonstrated two times lower adhesion to Si compared to standard PDMS, allowing 3 square inch area high quality silicone/nanowire membrane mechanical release, preserving the growth Si substrate for a further re-use after chemical cleaning. The 90% transparent single-walled carbon nanotubes electrical contacts to the embedded n-GaP nanowires demonstrated mechanical and electrical stability. The presented methods can be used for the fabrication of large scale flexible inorganic optoelectronic devices.

A new method was developed for the metal-free cross-linking of silicone rubbers. This process uses azobisisobutyronitrile (AIBN) to selectively react with Si-H and vinyl groups as a free-radical initiator for the thermal curing of polymethylhydrosiloxane (PMHS) and polymethylvinylsiloxane (PMVS). The AIBN-initiated curing reaction between the Si-H groups of PMHS generated Si-O-Si and Si-Si cross-links. In contrast, PMVS was cured via the formation of C-C bonds through "methyl-vinyl" and "vinyl-vinyl" mechanisms. Curing reactions were performed at 80-120 °C in air and confirmed by 13C and 29Si solid state NMR analyses and swelling trials.

The platinum-catalyzed self-cross-linking of polymethylhydrosiloxane at RT in air was performed for the first time and proved by 1H, 13C, and 29Si SSNMR and swelling measurements. Quantum chemical modeling of possible structures was investigated. Platinum (0) and (ii) complexes were used as catalysts between the Si-H groups of polymethylhydrosiloxane. Karstedt's catalyst leads to Si-O-Si and Si-Si bond formation, but cis-[PtCl2(BnCN)2] generates predominantly Si-O-Si cross-links. cis-[PtCl2(BnCN)2] allows creating high-quality silicone rubbers without visible mechanical defects. This cross-linking approach can be used to obtain new Si-H-containing silicone materials.

This study focuses on the synthesis of hybrid luminescent polysiloxanes and silicone rubbers grafted by organometallic rhenium(I) complexes using Cu(I)-catalyzed azido-alkyne cycloaddition (CuAAC). The design of the rhenium(I) complexes includes using a diimine ligand to create an MLCT luminescent center and the introduction of a triple C≡C bond on the periphery of the ligand environment to provide click-reaction capability. Poly(3-azidopropylmethylsiloxane-co-dimethylsiloxane) (N3-PDMS) was synthesized for incorporation of azide function in polysiloxane chain. [Re(CO)3(MeCN)(5-(4-ethynylphenyl)-2,2′-bipyridine)]OTf (Re1) luminescent complex was used to prepare a luminescent copolymer with N3-PDMS (Re1-PDMS), while [Re(CO)3Cl(5,5′-diethynyl-2,2′-bipyridine)] (Re2) was used as a luminescent cross-linking agent of N3-PDMS to obtain luminescent silicone rubber (Re2-PDMS). The examination of photophysical properties of the hybrid polymer materials obtained show that emission profile of Re(I) moiety remains unchanged and metallocenter allows to control the creation of polysiloxane-based materials with specified properties.

Cyclic organosilicon triperoxides were found to be vinyl-selective free-radical initiators for thermal curing at 100–180 °C of vinyl-terminated polydimethylsiloxane and trimethylsilyl-terminated polymethylhydrosiloxane producing homogeneous transparent silicone rubbers with antibacterial properties. The usage of the cyclic organosilicon triperoxides as the curing agents does not require free radical inhibitors in comparison with diacyl- and dialkyl peroxides. Among the tested compounds, the peroxide with the Me–Si–Me fragment and two cyclohexane rings is a much more active curing agent (180 °C, c = 0.22 M, τcuring = 45 min) than other organosilicon peroxides. Cured silicone samples from mixtures with vinyl-terminated polysiloxane and silicone hydride have improved mechanical properties: peroxides provide more than 200% elongation, and compression sets of the samples are less than 1%. The prepared silicone rubbers showed pronounced antibacterial activity.

Hydrosilylation catalyzed by the rhodium(I) complex [Rh(acac)(CO)2] or platinum(0)-based Karstedt's catalyst was employed to combine hydrophilic propargylated hydroxyethyl cellulose and hydrophobic hydride-terminated polydimethylsiloxane to give polymer hybrid structures. The final polymers were characterized by FTIR, solid state 1H, 13C and 29Si NMR, contact angle, microcalorimetry and thermogravimetry measurements. The grafting degree was controlled by the catalyst choice and by the reagent load variations; an increase of the polysiloxane load and a change from Karstedt's to the rhodium catalyst led to a higher (from 2 to 7%) silicon content in the glycosilicones. The glycosilicones were insoluble in water, but swelled in organic solvents (DMSO, DMF, and chloroform). The hydrophilicity of the glycosilicones decreased with incrementing silicon content: the contact angles increased from 30 (cellulose) to 103-131° in the hybrids. The glycosilicones obtained via the hydrosilylation are less toxic toward algae Chlorella vulgaris and infusoria Paramecium caudatum than those obtained with CuAAC.

This work proposes new chemical and mechanical materials and techniques for III-V semiconductor NW/silicone membrane formation and optoelectronic device fabrication. Molecular beam epitaxy (MBE)-synthesized n-, p- and i-GaP NWs were encapsulated by introduced G-coating method into synthesized polydimethylsiloxane- graft -polystyrene and released from the Si growth substrate. The fabricated membranes were contacted with different materials including single-walled carbon nanotubes or ferrocenyl-containing polymethylhydrosiloxane with and without multi-walled carbon nanotubes doping. The electrical connection of the fabricated membranes was verified by electron beam induced current (EBIC) spectroscopy. The developed methods and materials can be applied for fabrication of high quality flexible inorganic optoelectronic devices.

The reaction of 3,4-diaryl-1H-pyrrol-2,5-diimines with cis-dichlorobis(isonitrile)platinum(II) affords the C,N-chelated diaminocarbene platinum(II) complexes, which have been fully characterized including molecular spectroscopy, single crystal X-ray diffraction and DFT calculations. The obtained platinum(II) complexes are effective catalysts for the hydrosilylation of alkynes and alkenes. Thus, the reaction of phenylacetylene with triethoxysilane leads to the formation of α- and β-(E)-vinylsilanes, generating TON's in the range of 103 to 104 and TOF's in the range of 102 to 103 h−1. Also, the cross-linked silicones, possessing the luminescence properties, were obtained by the hydrosilylation reaction of vinyl- and hydride-containing polysiloxanes. Additionally, the efficiency of diaminocarbene platinum(II) complexes against CH1/PA-1, SW480, and A549 cancer cell lines has been demonstrated by in vitro cytotoxicity studies.

Experimental data on the application of metal complexes in radical polymerization of vinyl monomers collected over the recent 15 years have been analyzed and generalized. Special attention has been given to (un)substituted ferrocenes, macrocyclic (clathro)chelates, and iron porphyrinates as well as to the approaches to enhance their catalytic activity in controlled synthesis of macromolecules. The mentioned systems have been compared with each other as well as with selected complexes of other transition metals. It has been shown that the electronic and spatial structures of the metal complexes are related to their efficiency in the radical polymerization reactions.

The effect of the binary catalytic systems [the Karstedt catalyst–platinum(II) isocyanide complex] of the cure of vinyl-containing polydimethylsiloxane and hydride-containing siloxane oligomer via the hydrosilylation reaction has been studied.

The nitrile complexes trans-[PtCl2 (RCN)2 ] (R=Et (NC1), tBu (NC2), Ph (NC3), p-BrC6 H4 (NC4)) and cis-[PtCl2 (RCN)2 ] (R=Et (NC5), tBu (NC6), Ph (NC7)) react with 1 equiv of the hydroxyguanidine OC4 H8 NC(=NOH)NH2 (HG) furnishing the mono-addition products trans- and cis-[PtCl2 (RCN){NH=C(R)ON=C(NH2 )NC4 H8 O}] (1-4 and 9-11; 7 examples; 54-74 % yield). Treatment of any of the nitrile complexes NC1-NC7 with HG in a 1:2 molar ratio generated the bis-addition products trans- and cis-[PtCl2 {NH=C(R)ON=C(NH2 )NC4 H8 O}2 ] (5-8 and 12-14; 7 examples; 69-89 % yield). The PtII -mediated coupling between nitrile ligands and HG proceeds substantially faster than the corresponding reactions involving amid- and ketoximes and gives redox stable products under normal conditions. Complexes 1, 6⋅4 CH2 Cl2 , 7⋅4 CH2 Cl2 , 8⋅2 CH2 Cl2 , and NC4 were studied by X-ray crystallography. Platinum(II) species 1-3, 10, 11, and especially 9, efficiently catalyze the hydrosilylation cross-linking of vinyl-terminated poly(dimethylsiloxane) and trimethylsilyl-terminated poly(dimethylsiloxane-co-ethylhydrosiloxane) giving high-quality thermally stable silicon resins with no structural defects. The usage of these platinum species as the catalysts does not require any inhibitors and, moreover, the complexes and their mixtures with vinyl- and trimethylsilyl-terminated polysiloxanes are shelf-stable in air.

Cyclic peroxides as initiators for the radical polymerization of methyl methacrylate were proposed. The initial rates, initiation rates, and effective activation energies of polymerization initiated by cyclic peroxides and cyclic peroxide-1-pyridyl-2-ferrocene systems were determined. The radical yields to the volume upon the thermal decomposition of cyclic peroxides and their catalytic decomposition in the presence of 1-pyridyl-2-ferrocene were determined. In combination with 1-pyridyl-2-ferrocene cyclic peroxides form efficient initiating systems favoring an increase in the polymerization rate, a decrease in the molecular weights, and an increase in syndiotacticity of the synthesized poly(methyl methacrylate). © 2013 Springer Science+Business Media New York.

Physicochemical methods were used to study the interaction of arabinogalactan from Siberian larch with the antibacterial preparation levofloxacin. Polymeric eye films with controllable output of the medicinal preparation were produced on the basis of an arabinogalactan-polyvinyl alcohol formulation. A high pharmaceutical activity of the new eye films was demonstrated.

The effect of initiating systems based on substituted and unsubstituted metallocenes; polynuclear macrocyclic semi- and clathrochelates of Fe(II); and metal complexes of Ti(IV), Zr(IV), Fe(III), and Co(III) porphyrins on the free-radical polymerization of MMA and styrene is analyzed. Experimental data are systematized, general relationships are ascertained, and specific features of the process related to the structure of metal-complex compounds and the nature of initiators and monomers are revealed.

200 The use of metal complex compounds in radical polymerization of vinyl monomers is one of the most successful and promising ways of development of tai lor made synthesis of polymers on their basis [1, 2]. It has been shown [3–6] that iron(II) semi and clathro chelates in combination with traditional initiators of radical polymerization (in particular, diacyl perox ides) form high performance initiating systems. Such systems have a favorable effect on both the kinetic parameters of the process (increase the initiation rate; under certain conditions, mitigate the detrimental gel effect; reduce the effective activation energy of poly merization; etc.) and the physicochemical character istics of the resulting polymers (variation of the molec ular weight from 300 thousand daltons to 4 million daltons, the increase in stereoregularity and thermal stability). In this context, the use of new types of clath rochelates, in particular, macrobicyclic cobalt(II) tris(α dioximate)s (Scheme 1, compounds 1–3), as modifying additives in the radical polymerization of methyl methacrylate (MMA) initiated by benzoyl per oxide seems to be promising. All these compounds dif fer from the previously studied cage iron(II) com plexes [3–6] in the nature of both the encapsulated metal ion and the apical and edge substituents.

Recently, controlled radical polymerization has become one of the most important methods for producing synthetic vinyl polymers. At the moment several techniques enabling such polymerizations exist, of which ATRP (atom transfer radical polymerization) and RATRP (reverse atom transfer radical polymerization) are the most commonly used ones. [1] The significant advantages of these polymerization techniques include the ability to polymerize polymers with controlled density and chain length, and narrow molecular weight distribution (MWD) in a controlled manner. A wide range of compounds as alkoxyamines, dithioesters, trithiocarbonates, xanthates and others were proposed as propagation regulators. Metalloorganic compounds of general formula MtnYL, where Mt transition metal (Cu, Fe, Ru, Re, Ni and others); Y – halogen anion (mainly chlorine or bromine); L – organic ligand (mostly 2,2’-bipyridine, 4,4’-bi-(5-nonyl)-2,2’-pyridine, triphenylphosphine) are of great interests also. The use of metal complexes of porphyrins in controlled radical polymerization could be very promising.[2-6] Thus, catalytic chain transfer to the monomer and catalytic inhibition were discovered in the polymerization of methacrylates carried out in the presence of cobalt porphyrins.[2-5] It was found by B.B. Wayland and M. Fryd that cobalt complex of tetramesitylporphyrin initiates polymerization of acrylates leading to the formation of homopolymers and block copolymers.[7-9] However, only few metal porphyrins, which are well-soluble in organic media, mainly, cobalt, rhodium, aluminum complexes, allowing the radical polymerization of vinyl monomers under controlled mode, have been studied by now.[7-11] The goal of this work was the study of radical polymerization of vinyl monomers (by the example of methyl methacrylate (MMA) and styrene) initiated by azo-bis-isobutironitrile (AIBN) or benzoyl peroxide (BP) in the presence of various porphyrins and their metal complexes.

Influence of 1-[pyridyl-2]-, 1-[quinolin-2-yl]-, 1-[acridin-9-yl]-, 1-[pyrazin-2-yl]-, and 1-[pyrimid-4-yl]ferrocenes on heat and thermomechanical properties of the produced poly(methyl methacrylate) has been studied.

The free-radical bulk homopolymerization of methyl methacrylate and styrene initiated by benzoyl peroxide or AIBN in the presence of heterocyclic derivatives of ferrocene is studied. It is shown that, in the case of the peroxide initiator, ferrocene derivatives form highly efficient initiation systems, which make it possible to polymerize methyl methacrylate at a high rate, to reduce the molecular mass of polymers, and to synthesize polymers with a high content of syndiotactic triads, while in the case of AIBN, such systems are not formed.

The effect of ferrocenyl-containing semi- and clathrochelates on radical polymerization of methyl methacrylate, initiated by benzoyl peroxide, and on molecular characteristics of the polymer formed was examined.

Benzoyl peroxide-, lauryl peroxide-, and AIBN-initiated free-radical polymerization of methyl methacrylate has been studied in bulk and solution in the presence of macrobicyclic iron(II) bis(ferrocenyl borate) tris(nioximate). It has been found that the ferrocenyl-containing iron(II) clathrochelate forms efficient initiating systems with peroxides, whereas, in the case of AIBN, its presence has no effect on the kinetic parameters of the process and the properties of the resulting polymer. The use of clathrochelate complex-peroxide initiator systems accelerates the polymerization of methyl methacrylate and decreases the molecular mass of the polymer. The kinetic parameters of the process have been determined.

Radical polymerization of methyl methacrylate initiated by the benzoyl peroxide — macrobicyclic bis-ferrocenylboron-capped iron(ii) tris-1,2-cyclohexanedione dioximate system was studied. The ferrocenyl-containing macrobicyclic complex and benzoyl peroxide forms an efficient initiating system that allows one to perform the polymerization process at a high rate with substantially reduced amounts of the initiator and the metal complex component at 30–75 °C and to influence the molecular-weight characteristics of poly(methyl methacrylate) produced.

The free-radical polymerization of methyl methacrylate in the presence of chlorine-containing complexes of Fe(III) with 5,10,15,20-tetrakis(3′,5′-di-tert-butylphenyl)porphyrin and 5,10,15,20-tetrakis(3′-butoxyphenyl)porphyrin, as well as in the presence of the acetate complex of Co(III) 5,10,15,20-tetrakis(3′,5′-di-tert-butylphenyl)porphyrin, has been investigated. The kinetic features of the process and the molecular mass characteristics of polymers are studied, and a feasible polymerization mechanism is proposed.

Radical polymerization of methyl methacrylate and styrene initiated by azo-bis-isobutironitrile or benzoyl peroxide in the presence of chlorine-containing complexes of FeIII with 5,10,15,20-tetrakis-(3’,5’-di-tert-butylphenyl)porphyrin, 5,10,15,20-tetrakis-(3’-butoxyphenyl)porphyrin or 5,15-bis(4’-tert-butylphenyl)-2,8,12,18-tetra(n-butyl)-3,7,13,17tetramethylporphyrin and acetate complexes of CoIII with 5,10,15,20-tetrakis-(3’,5’-di-tert-butylphenyl)porphyrin or 5,10,15,20-tetrakis-(3’-butoxyphenyl)porphyrin and complex of CoII with 5,15-bis(4’-tert-butylphenyl)-2,8,12,18tetra(n-butyl)-3,7,13,17-tetramethylporphyrin were investigated. The kinetic features of the process and molecular mass characteristics of polymers were studied. Feasible polymerization scheme was proposed.

The free-radical polymerization of methyl methacrylate initiated by the three-component system ferrocene-zirconocene dichloride-benzoyl peroxide has been studied. The kinetic features of the process, the interaction between components of the initiation system, and the molecular characteristics of the polymers have been investigated. In the case of the three-component initiation system, the content of syndiotactic fragments grows and the thermal stability of the polymers is improved compared to the products of polymerization carried out in the presence of solely a peroxide initiator.

A series of ferrocenylboron-capped tris-dioximate iron(ii) clathrochelates was synthesized by the template condensation of three molecules of dimethylglyoxime (H2Dm), cyclohexanedione 1,2-dioxime (H2Nx), or cyclooctanedione 1,2-dioxime (H2Ox) and two molecules of ferrocenylboronic acid (FcB(OH)2) on the Fe2+ ion matrix. The yields of the clathrochelate derivatives of alicyclic dioximes were substantially higher than that of their acyclic analog, because the molecules of alicyclic H2Nx and H2Ox α-dioximes have the s-cis-configuration suitable for complex formation, whereas the H2Dm molecules in solution have the s-trans-configuration. The synthesized compounds were characterized using elemental analysis, IR and UV-Vis spectroscopies, MALDI-TOF mass spectrometry, 1H and 13C{1H} NMR and 57Fe Mossbauer spectroscopies, and X-ray diffraction analysis. The crystal of FeDm3(BFc)2·CHCl3 contains two types of crystallographically nonequivalent clathrochelate molecules. The intermolecular contacts C-H⋯Cp formed by the ferrocenyl fragments and cyclooctane carbocycles and the interactions Cp-H⋯O were observed in the crystal of FeOx3(BFc)2. The structural lability of the cyclooctane substituents allows the FeOx3(BFc)2 molecules to arrange by the “bump-into-hollow” mode because of attractive H⋯H interactions between the ribbed substituents of the neighboring molecules. The geometry of the ferrocenylborate iron(ii) clathrochelates is intermediate between a trigonal prism and a trigonal antiprism.

The direct template macrocyclization of 2,3-butanedione monooxime hydrazone (HDXO) with ferrocenylboronic acid on the iron(ii) ion matrix afforded the ferrocenylboron-capped semiclathrochelate iron(ii) oximehydrazonate. The H+ ion-catalyzed macrocyclization of this precursor with an excess of triethyl orthoformate gave the clathrochelate complex with syn,syn,syn-orientation of the ethoxy substituents relative to the 1,3,5-triazacyclohexane ring. The complexes synthesized were characterized using elemental analysis, IR and UV—Vis spectroscopies, MALDI-TOF mass spectrometry, 1H and 13C{1H} NMR, 57Fe Mossbauer spectroscopies, and X-ray diffraction analysis.