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Inne
Low pH constructed Co(II) and Ni(II) 1D coordination polymers based on C∝-substituted analogues of zoledronic acid: structural characterization, and spectroscopic and magnetic properties.
Autorzy
Rok wydania
2019
Czasopismo
Numer woluminu
9
Strony
31497-31510
DOI
10.1039/c9ra05673d
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Streszczenie
Three novel coordination compounds based on α,α-disubstituted analogues of zoledronic acid with a cyclopropane (cpp) or cyclobutane (cbt) ring on the Cα carbon, isomorphous [Co(H2cppZol)(H2O)]·H2O (1a), [Ni(H2cppZol)(H2O)]·H2O (1b) and [Co(H2cbtZol)(H2O)]·H2O (2a), were synthesized under hydrothermal conditions at low pH. Single-crystal X-ray diffraction analysis revealed that all the compounds had a 1D double zig–zag chain architecture with an 8 + 8 ring motif formed by alternately arranged symmetrical (–O–P–O–)2 bridges linking equivalent octahedral metal centres. Both the ligand coordination mode and chain architecture displayed by 1a, 1b and 2a are unique among 1D [M(H2L)(H2O)x]·yH2O coordination polymers based on nitrogen-containing bisphosphonates reported so far. All the compounds exhibit similar decomposition pathways upon heating with thermal stabilities decreasing in the order 1b > 1a > 2a. The IR spectra revealed that lattice water release above 227, 178 and 97 °C, respectively, does not change the chain architecture leaving them intact up to ca. 320, 280 and 240 °C. Magnetic behaviour investigations indicated that 1a, 2a and 1b exhibit weak alternating antiferromagnetic–ferromagnetic exchange interactions propagated between the magnetic centres through double (–O–P–O–)2 bridges. The boundary between antiferro- and ferromagnetic couplings for the Co–O⋯O–Co angle in 1a and 2a was estimated to be ca. 80°. This value is also applicable for recently reported [M3(HL)2(H2O)6]·6H2O (M = Co, Ni) complexes based on α,α-disubstituted analogues of zoledronic acid and can be used to the explain magnetic behaviour of 1b.
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Pełny tekst licencji: https://creativecommons.org/licenses/by-nc/4.0/legalcode
Adres publiczny
http://dx.doi.org/10.1039/c9ra05673d
Strona internetowa wydawcy
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