Supramolecular isomerism in the system [Crown-Ether.H3O]MF6 (M= Ta, Nb)
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FURMANOVA, N, VERIN, I., GELMBOLDT, Vladimir, GANIN, Eduard, WANG, Wen-Jwu, SIMONOV, Yurii A., FONARI, Marina. Supramolecular isomerism in the system [Crown-Ether.H3O]MF6 (M= Ta, Nb). In: Physical Methods in Coordination and Supramolecular Chemistry, 27 septembrie - 1 octombrie 2006, Chişinău. Chisinau, Republic of Moldova: 2006, XVII, p. 126. ISBN 978-9975-62-066-6.
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Physical Methods in Coordination and Supramolecular Chemistry
XVII, 2006
Conferința "The XV-th International Conference Physical Methods in Coordination and Supramolecular Chemistry : The XVII-th Reading in memory of Acad. A.Ablov"
Chişinău, Moldova, 27 septembrie - 1 octombrie 2006

Supramolecular isomerism in the system [Crown-Ether.H3O]MF6 (M= Ta, Nb)


Pag. 126-126

Furmanova N1, Verin I.2, Gelmboldt Vladimir3, Ganin Eduard4, Wang Wen-Jwu5, Simonov Yurii A.6, Fonari Marina6
 
1 Institutul de Cristalogie,
2 A.V.Shubnikov Institute of Crystallography, Moscow,
3 Odessa State Environmental University,
4 Physicochemical Institute of Environmental Protection and Human, Odessa,
5 Tamkang University Tamsui, Taipei Taiwan (ROC),
6 Institute of Applied Physics
 
 
Disponibil în IBN: 10 iunie 2020


Rezumat

Supramolecular isomerism (SI)  in coordination polymers has received increasing interest n recent years for fundamental and applied reasons [1]. he occurrence of SI implies superstructural diversity for a given building block. We report the crystal structures a given building block. We report the crystal structures  or the systems, [CE(crown-ether).H O]MF (M=Ta, Nb), f 3 6 where CE=benzo-18C6, cis-syn-cis-DCH18C6, which afford novel examples of SI. It was stated the influence of the synthetic route on the crystallography of the final product: the interaction of Ta2O5 with HF in the presence of corresponding CE results in the monoclinic modifications regardless of CE used (P2 /n both), while interaction of TaF with CE in the medium of HF results in an orthorhombic isomer for [B18C6.H3O]TaF6 (Pbca) and triclinic one (P-1)  for [DCH18C6.H3O]TaF6. For these latter complexes the isostructural Nb counterparts were obtained. For [B18C6. H3O]TaF6 the distinction between the isomers is dictated by the packing conditions of the quite similar building blocks (fig.), while in [DCH18C6.H3O]TaF6 the macrocyclic molecule exhibits strictly different conformations in  monoclinic and triclinic modifications [2,3]. schemeMonoclinic and orthorhombic isomers for [B18C6.H3O]TaF6

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<cfAbstr cfLangCode='EN' cfTrans='o'><p>Supramolecular isomerism (SI)&nbsp;&nbsp;in coordination polymers has received increasing interest&nbsp;n recent years for fundamental and applied reasons [1].&nbsp;he occurrence of SI implies superstructural diversity for&nbsp;a given building block. We report the crystal structures&nbsp;a given building block. We report the crystal structures&nbsp; or the systems, [CE(crown-ether).H O]MF (M=Ta, Nb), f 3 6 where CE=benzo-18C6, cis-syn-cis-DCH18C6, which&nbsp;afford novel examples of SI. It was stated the influence&nbsp;of the synthetic route on the crystallography of the final product: the interaction of Ta2O5 with HF in the presence of&nbsp;corresponding CE results in the monoclinic modifications regardless of CE used (P2 /n both), while interaction of TaF&nbsp;with CE in the medium of HF results in an orthorhombic isomer for [B18C6.H3O]TaF6 (Pbca) and triclinic one (P-1)&nbsp;&nbsp;for [DCH18C6.H3O]TaF6. For these latter complexes the&nbsp;isostructural Nb counterparts were obtained. For [B18C6.&nbsp;H3O]TaF6 the distinction between the isomers is dictated by&nbsp;the packing conditions of the quite similar building blocks&nbsp;(fig.), while in [DCH18C6.H3O]TaF6 the macrocyclic&nbsp;molecule exhibits strictly different conformations in&nbsp; monoclinic and triclinic modifications [2,3].&nbsp;</p><p>scheme</p><p>Monoclinic and orthorhombic isomers&nbsp;for [B18C6.H3O]TaF6</p></cfAbstr>
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