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Outerly functionalized and non-functionalized boron clusters intercalated into layered hydroxides with different modes of binding: materials for superacid storage
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SYSNO ASEP 0492890 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Outerly functionalized and non-functionalized boron clusters intercalated into layered hydroxides with different modes of binding: materials for superacid storage Author(s) Melánová, Klára (UMCH-V) RID, ORCID
Holub, Josef (UACH-T) SAI, RID, ORCID
Hynek, Jan (UACH-T) SAI, RID, ORCID
Fanfrlík, Jindřich (UOCHB-X) RID, ORCID
Beneš, L. (CZ)
Kutálek, P. (CZ)
Krejčová, A. (CZ)
Hnyk, Drahomír (UACH-T) SAI, RID, ORCID
Zima, Vítězslav (UMCH-V) RID, ORCIDSource Title Dalton Transactions. - : Royal Society of Chemistry - ISSN 1477-9226
Roč. 47, č. 33 (2018), s. 11669-11679Number of pages 11 s. Language eng - English Country GB - United Kingdom Keywords boranes ; carboranes ; intercalation Subject RIV CD - Macromolecular Chemistry OECD category Polymer science Subject RIV - cooperation Institute of Inorganic Chemistry - Inorganic Chemistry
Institute of Organic Chemistry and Biochemistry - Physical ; Theoretical ChemistryR&D Projects GA17-10639S GA ČR - Czech Science Foundation (CSF) GA17-08045S GA ČR - Czech Science Foundation (CSF) Institutional support UMCH-V - RVO:61389013 ; UACH-T - RVO:61388980 ; UOCHB-X - RVO:61388963 UT WOS 000442509700040 EID SCOPUS 85051949285 DOI 10.1039/C8DT02251H Annotation Two binary boron hydrides (NH4)2B10H10 and Na2B12H12 and mono- and dicarboxy p- and m-carboranes (namely, 1-(COOH)-closo-1,7-C2B10H11, 1,12-(COOH)2-closo-1,12-C2B10H10 and 1,7-(COOH)2-closo-1,7-C2B10H10) were intercalated into ZnAl-layered double hydroxides (ZnAl-LDH) and into Zn5(OH)8(NO3)2·2H2O. The formed compounds were characterized using elemental analysis, thermogravimetry analysis, X-ray powder diffraction, infrared spectroscopy and solid state NMR. All the intercalated boron compounds are present in the interlayer space of the layered hosts as anions. It is presumed that in the case of B10H102−, B12H122− and 1,12-(COO)2-closo-1,12-C2B10H102−, the guest molecules form a monolayer, whereas in the case of 1-(COO)-closo-1,7-C2B10H111− and 1,7-(COO)2-closo-1,7-C2B10H102− a bilayer arrangement is more probable. In the case of 1,7-(COO)2-closo-1,7-C2B10H102−, the guest molecules are strongly interdigitated resulting in lowering of the interlayer distance. Two different modes of binding were found. Whereas the carboxylate derivatives of p- and m-carboranes are bonded through classical hydrogen bonds, the corresponding parent borane anions interact with the host structures by mainly dihydrogen bonding. In effect, both kinds of hydrogen bonding are mainly of an electrostatic nature. The dihydrogen bond is detected, e.g. in crystal engineering, and represents a driving force for interactions of boranes with biomolecules. Since the latter dicarboxylic acids were found to be superacids, their interactions with the host structures should be stronger than in the case of the benzoic and terephthalic acid intercalates. Workplace Institute of Macromolecular Chemistry Contact Eva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358 Year of Publishing 2019
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