閲覧可能ファイル 

ファイル	フォーマット	サイズ	閲覧回数	説明
Ali_ChemCatChem-yellow	pdf	392 KB	2,092

論文情報

ファイル出力 EndNote Basic出力 Mendeley出力

アクセス権	open access
URI	https://hdl.handle.net/2115/64656
タイトル	Direct Synthesis of Cyclic Imides from Carboxylic Anhydrides and Amines by Nb2O5 as a Water-Tolerant Lewis Acid Catalyst
著者	Ali, Md. A. ; Moromi, Sondomoyee K. ; Touchy, Abeda S. ; Shimizu, Ken-ichi
著者名 Ali, Md. A.
著者名 Moromi, Sondomoyee K.
著者名 Touchy, Abeda S.
e-Rad_Researcher 60324000 著者名 Shimizu, Ken-ichi
言語	英語
キーワード	amination
	ketones
	Lewis acids
	niobium
	primary amines
発行日	2016-03-07
出版者	Wiley-VCH
収録物名	ChemCatChem
巻(号)	8(5)
ページ	891-894
抄録	In the 20 types of heterogeneous and homogenous catalysts screened, Nb2O5 showed the highest activity for the synthesis of N-phenylsuccinimide by dehydrative condensation of succinic anhydride and aniline. Nb2O5 was used in the direct imidation of a wide range of carboxylic anhydrides with NH3 or amines with various functional groups and could be reused. Kinetic studies showed that the Lewis acid Nb2O5 catalyst was more water tolerant than both the Lewis acidic oxide TiO2 and the homogeneous Lewis acid ZrCl4, which resulted in higher yields of imides through the use of Nb2O5.
資源タイプ	学術雑誌論文
出版タイプ	Accepted Manuscript
権利情報	This is the peer-reviewed version of the following article: ChemCatChem, Vol.8(5), March 7, 2016 Pages 891–894, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/cctc.201501172/abstract. This article may be used for non-commercial purposes in accordance with Wiley-VCH Terms and Conditions for Self-Archiving.
PISSN	1867-3880
関連情報 (isVersionOf)	出版社版DOI https://doi.org/10.1002/cctc.201501172

ホームへ戻る