An Aluminum Hydride That Functions like a Transition-Metal Catalyst

作者: Zhi Yang , Mingdong Zhong , Xiaoli Ma , Susmita De , Chakkittakandiyil Anusha

DOI: 10.1002/ANIE.201503304

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摘要: The reaction of [LAlH2] (L=HC(CMeNAr)2, Ar=2,6-iPr2C6H3) with MeOTf (Tf=SO2CF3) resulted in the formation [LAlH(OTf)] (1) high yield. triflate substituent 1 increases positive charge at aluminum center, which implies that has a strong Lewis acidic character. excellent catalytic activity for hydroboration organic compounds carbonyl groups was investigated. Furthermore, it shown effectively initiates addition trimethylsilyl cyanide (TMSCN) to both aldehydes and ketones. Quantum mechanical calculations were carried out explore mechanism.

参考文章(37)
Joseph A. B. Abdalla, Ian M. Riddlestone, Rémi Tirfoin, Simon Aldridge, Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center Angewandte Chemie. ,vol. 54, pp. 5098- 5102 ,(2015) , 10.1002/ANIE.201500570
Mathew D. Anker, Merle Arrowsmith, Peter Bellham, Michael S. Hill, Gabriele Kociok-Köhn, David J. Liptrot, Mary F. Mahon, Catherine Weetman, Selective reduction of CO2 to a methanol equivalent by B(C6F5)3-activated alkaline earth catalysis Chemical Science. ,vol. 5, pp. 2826- 2830 ,(2014) , 10.1039/C4SC00885E
David R. Armstrong, Elaine Crosbie, Eva Hevia, Robert E. Mulvey, Donna L. Ramsay, Stuart D. Robertson, TMP (2,2,6,6-tetramethylpiperidide)-aluminate bases : lithium-mediated alumination or lithiation-alkylaluminium-trapping reagents? Chemical Science. ,vol. 5, pp. 3031- 3045 ,(2014) , 10.1039/C4SC01108B
Borislav Bogdanović, Manfred Schwickardi, Ti-doped alkali metal aluminium hydrides as potential novel reversible hydrogen storage materials Journal of Alloys and Compounds. ,vol. 253, pp. 1- 9 ,(1997) , 10.1016/S0925-8388(96)03049-6
Vojtech Jancik, Ying Peng, Herbert W. Roesky, Jiyang Li, Dante Neculai, Ana M. Neculai, Regine Herbst-Irmer, The First Structurally Characterized Aluminum Compound with Two SH Groups: [LAl(SH)2] (L = N(Ar)C(Me)CHC(Me)N(Ar), Ar = 2,6-i-Pr2C6H3) and the Catalytic Properties of the Sulfur P(NMe2)3 System Journal of the American Chemical Society. ,vol. 125, pp. 1452- 1453 ,(2003) , 10.1021/JA028801K
Alexander J. Blake, Anthony Cunningham, Alan Ford, Simon J. Teat, Simon Woodward, Enantioselective reduction of prochiral ketones by catecholborane catalysed by chiral group 13 complexes Chemistry: A European Journal. ,vol. 6, pp. 3586- 3594 ,(2000) , 10.1002/1521-3765(20001002)6:19<3586::AID-CHEM3586>3.0.CO;2-S
Falguni Basuli, Halikhedkar Aneetha, John C. Huffman, Daniel J. Mindiola, A Fluorobenzene Adduct of Ti(IV), and Catalytic Carboamination to Prepare α,β-Unsaturated Imines and Triaryl-Substituted Quinolines Journal of the American Chemical Society. ,vol. 127, pp. 17992- 17993 ,(2005) , 10.1021/JA0566026
Chunming Cui, Herbert W. Roesky, Haijun Hao, Hans-Georg Schmidt, Mathias Noltemeyer, The First Structurally Characterized Metal–SeH Compounds: [LAl(SeH)2] and [L(HSe)AlSeAl(SeH)L] Angewandte Chemie. ,vol. 112, pp. 1815- 1817 ,(2000) , 10.1002/(SICI)1521-3757(20000515)112:10<1885::AID-ANGE1885>3.0.CO;2-K