IR and UV study of reversible water-induced structural transformations of poly(manganese 1,1′-ferrocenediyl-bis(H-phosphinate)) and poly(cobalt 1,1′-ferrocenediyl-bis(H-phosphinate))

被引:13
|
作者
Gerasimova, Tatiana [1 ]
Shekurov, Ruslan [1 ]
Gilmanova, Leysan [1 ]
Laskin, Artem [2 ]
Katsyuba, Sergey [1 ]
Kovalenko, Valeri [1 ]
Khrizanforov, Mikhail [1 ]
Milyukov, Vasiliy [1 ]
Sinyashin, Oleg [1 ]
机构
[1] Russian Acad Sci, Kazan Sci Ctr, AE Arbuzov Inst Organ & Phys Chem, Lab Phys Chem Anal, Arbuzov Str 8, Kazan 420088, Russia
[2] Kazan Fed Univ, Alexandr Butlerov Inst Chem, Lab Ind Catalysis, Kremlevskaya Str 29-1, Kazan 420008, Russia
关键词
Metal-organic frameworks; Ferrocenylphosphinic acids; UV-Vis and vibrational spectroscopy; Crystal-to-amorphous transformation; METAL-ORGANIC FRAMEWORKS; NANOSCALE COORDINATION POLYMERS; CRYSTAL-STRUCTURE; FERROCENYLPHOSPHONIC ACID; COMPLEXES; DESIGN; MANGANESE(II); SPECTRA; HALIDES; SOLIDS;
D O I
10.1016/j.molstruc.2018.04.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recently new flexible and hydrolytically stable metal-organic framework [M(H2O)(2)(Fc(PHOO)(2))center dot 2H(2)O](n) M = Co has been synthesized by the use of synthetic technique, described earlier for M = Mn [1]. The heating of both complexes leads to elimination of water molecules and in the case of Co complex is accompanied by change of its color from orange to dark blue. The corresponding structural changes are reversible and are reflected in vibrational and electronic absorption spectra. Analysis of IR, Raman and UV-vis spectra of complexes shows the same structures of Mn and Co complexes before and after heating and suggests that both Mn and Co coordination polyhedra undergo reversible changes under heating from octahedral to tetrahedral form with ferrocene part remaining unchanged. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:237 / 242
页数:6
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