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RESEARCH PRODUCT
Supramolecular Assembly of Organophosphonate Diesters Using Paddle-Wheel Complexes: First Examples in Porphyrin Series
Roman ZubatyukYulia EnakievaAslan TsivadzeOleg ShishkinMarina UvarovaAnna SinelshchikovaMargarita GolubnichayaSergey NefedovYulia Yu. EnakievaYulia G. GorbunovaAslan Yu. TsivadzeChristine SternAlla Bessmertnykh-lemeuneRoger Guilardsubject
010405 organic chemistryStereochemistryChemistryLigandchemistry.chemical_elementGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesPorphyrin0104 chemical sciencesSupramolecular assemblychemistry.chemical_compoundNickelPaddle wheelPolymer chemistry[CHIM]Chemical SciencesMoietyGeneral Materials ScienceComputingMilieux_MISCELLANEOUSTriphenylphosphine oxidePalladiumdescription
The reactions of dicopper tetrapivalate complex Cu2(μ-OOC-t-Bu)4(NCMe)2 (1) with triphenylphosphine oxide and diethyl phosphite allow paddle-wheel (PW) copper(II) complexes with phosphorus-containing axial ligands (2, 3) to be obtained. When meso-bis(diethoxyphosphoryl)porphyrins 4M were employed in this ligand exchange reaction, a series of one-dimensional (1D) homo- and heterometallic coordination polymers 5M composed of PW subunits and organophosphonate diesters were prepared and characterized by means of single crystal X-ray analysis. Planar porphyrinate 4Pd and nonplanar metalloporphyrinates 4Cu and 4Ni proved to be appropriate molecular structural blocks for assembly of coordination polymers. The structural parameters of the tetrapyrrolic macrocycles incorporated into the polymer chain are determined by the nature of the metal center of the porphyrin moiety. While the geometry of palladium(II) and nickel(II) porphyrinates 4Pd and 4Ni does not change significantly in the polymer chain, saddle-shaped ...
year | journal | country | edition | language |
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2014-10-06 | Crystal Growth & Design |