Dimeric alumatranes as catalysts for trimethylsilylcyanation reactionElectronic supplementary information (ESI) available: NMR, IR, EI mass spectra and computational details. CCDC 1494116-1494118. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ra09851k

The solid-state structures of dimeric alumatranes with three five-membered rings chelated by [(OCMe 2 CH 2 ) n N(CH 2 CH 2 O) 3− n ] 3− ( n = 1, L1 ; n = 2, L2 ; n = 3, L3 ), which vary by the number of CMe 2 groups adjacent to the OH functionality [ 1 ( L1H 3 ), 2 ( L2H 3 ), and 3 ( L3H 3 )], were...

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Main Authors: Kim, Yoseph, Lee, Kang Mun, Kim, So Han, Moon, Jung Hee, Kim, Youngjo
Format: Journal Article
Language:English
Published: 13-10-2017
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Summary:The solid-state structures of dimeric alumatranes with three five-membered rings chelated by [(OCMe 2 CH 2 ) n N(CH 2 CH 2 O) 3− n ] 3− ( n = 1, L1 ; n = 2, L2 ; n = 3, L3 ), which vary by the number of CMe 2 groups adjacent to the OH functionality [ 1 ( L1H 3 ), 2 ( L2H 3 ), and 3 ( L3H 3 )], were determined by single-crystal X-ray diffraction. The X-ray structures revealed that the aluminum geometries were slightly distorted trigonal bipyramids. The obtained aluminum complexes are the first structurally characterized dimeric alumatranes with tricyclic five-membered rings. Quite unexpectedly, the sterically bulky side arms with dimethyl substituents were always located in the bridging sites, as determined by density functional theory calculations. Their solution-state structures were analyzed by 1 H, 13 C, and 27 Al NMR techniques, and their gas-phase structures were determined by mass spectrometry. Unlike Al(OCH 2 CH 2 ) 3 N, complexes 1-3 were all dimeric in the solid state, solution phase, and gas phase. In addition, they were found to promote the reaction of aryl, heteroaryl, and alkyl aldehydes with trimethylsilylcyanide to provide the corresponding products in excellent yields under mild conditions of room temperature, a short reaction time of 1 h, and a very low catalyst loading of 0.5 mol%. First structurally characterized dimeric alumatranes with tricyclic five-membered rings were determined by single-crystal X-ray analysis and DFT calculations. New alumatranes were used as catalysts for trimethylsilycyanation reaction of aldehydes.
Bibliography:Electronic supplementary information (ESI) available: NMR, IR, EI mass spectra and computational details. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
1494116-1494118
10.1039/c7ra09851k
ISSN:2046-2069
DOI:10.1039/c7ra09851k