η1-Ligation versus Pnictogen−Carbon Double Bond Cleavage: The Contrasting Behavior of Phospha- and Arsaalkenes [Tp*(CO)2M⋮C−EC(NMe2)2] [E = P, As; M = Mo, W; Tp* = HB(3,5-Me2pz)3] toward [Au(CO)Cl]
Author:
Affiliation:
1. Fakultät für Chemie der Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany, and Institut für Anorganische Chemie der Universität Leipzig, Johannisallee 29, D-04103 Leipzig, Germany
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om010071m
Reference35 articles.
1. (a) Dillon, K. B.; Mathey, F.; Nixon, J. F.Phosphorus: The Carbon Copy; Wiley: Chichester, 1998, pp 88−127.
2. Metallophosphaalkene – von Außenseitern zu vielseitigen Bausteinen in der präparativen Chemie
3. Review: Weber, L.Chem. Ber.1996,129, 367, and references therein.
4. Metalloarsaalkene [(η5-C5Me5)(CO)2FeAs=C(NMe2)2] as a Ligand in Carbonylchromium, -iron, and -nickel Complexes
5. Transition metal-substituted phosphaalkenes and acylphosphanes. XXIX. Metallophosphaalkene (η5-C5Me5)(CO)2FePC(NMe2)2, a versatile molecule in coordination chemistry
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