Synthesis, characterization, and crystal structures of [N(CH3)(4)](2)[B12H12] and [N(CH3)(4)](2)[B12H12]center dot CH3CN

Citation
K. Hofmann et B. Albert, Synthesis, characterization, and crystal structures of [N(CH3)(4)](2)[B12H12] and [N(CH3)(4)](2)[B12H12]center dot CH3CN, Z ANORG A C, 627(5), 2001, pp. 1055-1058
Citations number
31
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
ISSN journal
00442313 → ACNP
Volume
627
Issue
5
Year of publication
2001
Pages
1055 - 1058
Database
ISI
SICI code
0044-2313(200105)627:5<1055:SCACSO>2.0.ZU;2-H
Abstract
Bis(tetramethylammonium) dodecahydrododecaborate, [(CH3)(4)N](2)[B12H12], a nd bis(tetramethylammonium) dodecahydrododecaborate acetonitrile, [(CH3)(4) N](2)[B12H12]. CH3CN, were synthesized and characterized via Infrared,H-1 a nd B-11 NMR spectroscopy. [(CH3)(4)N](2)[B12H12] crystallizes isopunctual t o the alkali metal dodecaborates. The crystal structure of [(CH3)(4)N](2)[B 12H12]. CH3CN was determined from single crystal data and refined in the or thorhombic crystal system (Pcmn, no.62, a=898.68(8), b=1312.85(9) c = 1994. 5(1) pm, R([F], 4 sigma)= 5.9%, wR(F-2) = 18.3%). Here, the geometry of the dodecaborate anion is that of an almost ideal icosahedron, less distorted than most other dodecaborates known. By low-temperature Guinier-Simon diffr actometry phase transitions were detected for [(CH3)(4)N](2)[B12H12] and [( CH3)(4)N](2)[B12H12]. CH3CN at -70 and -15 degreesC, respectively.