The detection of PHIP effects allows new insights into the mechanism of olefin isomerisation during catalytic hydrogenation
…, D Santelia, R Napolitano, R Gobetto…
Index: Viale, Alessandra; Santelia, Daniela; Napolitano, Roberta; Gobetto, Roberto; Dastru, Walter; Aime, Silvio European Journal of Inorganic Chemistry, 2008 , # 28 p. 4348 - 4351
Full Text: HTML
Citation Number: 4
Abstract
Abstract PHIP (parahydrogen-induced polarisation) effects in the 1 H NMR spectra of the products of Rh-complex-catalysed alkyne hydrogenation brings to light the fact that the cis– trans isomerisation of the formed olefin occurs through the formation of a σ-bonded intermediate stabilised by the reversible addition of a hydrogen molecule at the metal centre.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Related Articles:
[Wu, Wen-Jin; Feng, Yuguo; He, Xiang; Hofstein, Hilary A.; Raleigh, Daniel P.; Tonge, Peter J. Journal of the American Chemical Society, 2000 , vol. 122, # 17 p. 3987 - 3994]
[Gaviglio, Carina; Doctorovich, Fabio Journal of Organic Chemistry, 2008 , vol. 73, # 14 p. 5379 - 5384]
[Amat, Ana M.; Asensio, Gregorio; Castello, Maria J.; Miranda, Miguel A.; Simon-Fuentes, Antonio Tetrahedron, 1987 , vol. 43, # 5 p. 905 - 910]
[Mohrig, Jerry R.; Carlson, Hans K.; Coughlin, Jane M.; Hofmeister, Gretchen E.; McMartin, Lea A.; Rowley, Elizabeth G.; Trimmer, Elizabeth E.; Wild, Andrew J.; Schultz, Steve C. Journal of Organic Chemistry, 2007 , vol. 72, # 3 p. 793 - 798]
[Rudler, Henri; Durand-Reville, Thomas Journal of Organometallic Chemistry, 2001 , vol. 617, # 1 p. 571 - 587]