Repozytorium

Two isomorphous Co(II) coordination polymers based on new α, α-disubstituted derivatives of zoledronic acid : synthesis, structures and properties.

Autorzy

Tomasz Rojek

Waldemar Goldeman

Katarzyna Ślepokura

Marek Duczmal

Agnieszka Wojciechowska

Ewa Matczak-Jon

Rok wydania

2017

Czasopismo

Dalton Transactions

Numer woluminu

46

Strony

6900-6911

DOI

10.1039/c7dt00410a

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Two novel α,α-disubstituted derivatives of zoledronic acid, namely 1-hydroxy-2-(1H-imidazol-1-yl)-2-methylpropylidene-1,1-diphosphonic acid (H4L1) and 1-hydroxy-2-[1-(1H-imidazol-1-yl)cyclopropyl]ethylidene-1,1-diphosphonic acid (H4L2) were synthesized and structurally characterized by single-crystal X-ray diffraction. The reaction of cobalt acetate with H4L1 and H4L2 carried out under hydrothermal conditions afforded two isomorphous Co3(HL1)2(H2O)6·6H2O (1a) and Co3(HL2)2(H2O)6·6H2O (2a) complexes. Both compounds are characterized by means of X-ray crystallography, IR and NIR–Vis–UV spectroscopic methods. Furthermore, their magnetic properties and thermal stabilities are reported. The crystals of 1a and 2a feature infinite 1D polymeric chains built from alternately arranged dinuclear [Co2(HL1/HL2)(H2O)2]2 units and {Co1O6} octahedra running along the [10] crystallographic direction. In both compounds, crystallographically distinct Co1 and Co2 atoms are six-coordinated. As is reflected in T values (T – index of tetragonality), the coordination environment of Co1 generates a slightly elongated octahedron (T = 0.94), whereas a slightly compressed octahedron (T = 1.06 for 1a and 1.05 for 2a) is formed around Co2. An assumption that the d–d type absorption is mainly attributed to the inversion related Co2 centers, whose population is two times higher than that of Co1, afforded a good correlation between calculated transition energies and experimental NIR–Vis–UV spectra. The magnetic susceptibility measurements analyzed in terms of a spin-3/2 Heisenberg trimer chain revealed that Co1⋯Co2 interactions within the trimer are antiferromagnetic whereas Co2⋯Co2 intertrimer interactions are ferromagnetic.

Adres publiczny

http://dx.doi.org/10.1039/c7dt00410a

Strona internetowa wydawcy

https://www.rsc.org/

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