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Darstellung und NMR-spektroskopische charakterisierung einiger di-n-alkyl- und n-alkylaryl-chlorphosphane
Affiliation:1. CNRS–ICARE, 1C avenue de la Recherche Scientifique, 45071 Orléans cedex 2, France;2. Collegium Sciences et Techniques, Université d’Orléans, rue de Chartres, 45100 Orléans, France;1. N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation;2. V. V. Voevodsky Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation;3. Department of Natural Sciences, National Research University – Novosibirsk State University, 630090 Novosibirsk, Russian Federation;4. Department of Physics, National Research University – Novosibirsk State University, 630090 Novosibirsk, Russian Federation;1. Institute of Petrochemistry and Catalysis of Russian Academy of Sciences, 141 Pr. Oktyabrya, Ufa 450075, Russian Federation;2. Chemistry, University of Southampton, Southampton SO17 1BJ, United Kingdom;1. State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China;2. National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8565, Japan;1. Chemical and Environmental Engineering Department, University College of Technical Mining and Civil Engineering, University of the Basque Country UPV/EHU, Rafael Moreno ''Pitxitxi'' 2, 48013 Bilbao, Spain;2. Chemical and Environmental Engineering Department, School of Engineering, University of the Basque Country UPV/EHU, Alameda de Urquijo s/n, 48013 Bilbao, Spain
Abstract:A series of di-n-alkyl and n-alkylaryl chlorophosphines has been prepared by the reaction of tetraorganodiphosphines with chlorodiphenyl or dichlorophenyl phosphine and characterized by 31P and 13C NMR spectra.
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