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Title: Synthesis and structure of a 1,6-hexyldiamine heptaborate, [H{sub 3}N(CH{sub 2}){sub 6}NH{sub 3}][B{sub 7}O{sub 10}(OH){sub 3}]

Journal Article · · Journal of Solid State Chemistry
 [1]; ;  [1];  [2];  [1]
  1. Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)
  2. China University of Geoscience, X-ray Laboratory, Beijing 100083 (China)

A new 1,6-hexyldiamine heptaborate, [H{sub 3}N(CH{sub 2}){sub 6}NH{sub 3}][B{sub 7}O{sub 10}(OH){sub 3}] (1), has been solvothermally synthesized and characterized by single-crystal X-ray diffraction, FTIR, elemental analysis, and thermogravimetric analysis. Compound 1 crystallizes in monoclinic system, space group P2{sub 1}/n with a=8.042(2) A, b=20.004(4) A, c=10.103(2) A, and {beta}=90.42(3) deg. The anionic [B{sub 7}O{sub 10}(OH){sub 3}]{sub n}{sup 2n-} layers are interlinked via hydrogen bonding to form a 3D supramolecular network containing large channels, in which the templated [H{sub 3}N(CH{sub 2}){sub 6}NH{sub 3}]{sup 2+} cations are located. - Graphical abstract: A layered 1,6-hexyldiamine heptaborate, [H{sub 3}N(CH{sub 2}){sub 6}NH{sub 3}][B{sub 7}O{sub 10}(OH){sub 3}], was solvothermally synthesized at 150 deg. C. It is a layer borate and crystallized in monoclinic space group P2{sub 1}/n with a=8.042(2) A, b=20.004(4) A, c=10.103(2) A, {beta}=90.42(3) deg.

OSTI ID:
21043798
Journal Information:
Journal of Solid State Chemistry, Vol. 180, Issue 8; Other Information: DOI: 10.1016/j.jssc.2007.05.029; PII: S0022-4596(07)00218-6; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0022-4596
Country of Publication:
United States
Language:
English