Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As)
Weber L, Scheffer MH, Stammler H-G, Neumann B, Schoeller W, Sundermann A, Laali K (1999)
Organometallics 18(20): 4216-4221.
Zeitschriftenaufsatz
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Autor*in
Weber, LotharUniBi;
Scheffer, Matthias H.;
Stammler, Hans-GeorgUniBi;
Neumann, BeateUniBi;
Schoeller, WolfgangUniBi;
Sundermann, A.;
Laali, Kenneth
Abstract / Bemerkung
Reaction of equimolar amounts of the metallophosphaalkene eta(5)-Cp*(CO)(2)FeP=C(NMe2)(2) (1a) and the metalloarsaalkene eta(5)-Cp*(CO)(2)FeAs=C(NMe2)(2) (1b) with ethereal HBF4 or the trifluoromethanesulfonates ROSO2CF3 (R = CH3, Me3SiCH2, Me3Si), respectively, afforded the phosphanyl-substituted carbenium salts [eta(5)-Cp*(CO)(2)FeP(R)C(NMe2)(2)]X (2a, R = H, X = BF4; 3a, R = CH3, X = SO3CF3; 4a, R = Me3SiCH2, X = SO3CF3; 5a, R = Me3Si, X = SO3CF3) as well as their arsenic analogues [eta(5)-Cp*(CO)(2)FeAs(R)C(NMe2)(2)]X (2b, R = H, X = BF4; 3b, R = CH3, X = SO3CF3; 4b, R = Me3SiCH2, X = SO3CF3; 5b, Me3Si, X = SO3CF3). The cations feature a trigonal-planar bis(amino)carbenium center, which is connected to a phosphorus or arsenic atom with pyramidal configuration. The molecular structure of 3b has been determined by X-ray diffraction analysis.
Erscheinungsjahr
1999
Zeitschriftentitel
Organometallics
Band
18
Ausgabe
20
Seite(n)
4216-4221
ISSN
0276-7333
eISSN
1520-6041
Page URI
https://pub.uni-bielefeld.de/record/1621620
Zitieren
Weber L, Scheffer MH, Stammler H-G, et al. Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As). Organometallics. 1999;18(20):4216-4221.
Weber, L., Scheffer, M. H., Stammler, H. - G., Neumann, B., Schoeller, W., Sundermann, A., & Laali, K. (1999). Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As). Organometallics, 18(20), 4216-4221. https://doi.org/10.1021/om990100h
Weber, Lothar, Scheffer, Matthias H., Stammler, Hans-Georg, Neumann, Beate, Schoeller, Wolfgang, Sundermann, A., and Laali, Kenneth. 1999. “Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As)”. Organometallics 18 (20): 4216-4221.
Weber, L., Scheffer, M. H., Stammler, H. - G., Neumann, B., Schoeller, W., Sundermann, A., and Laali, K. (1999). Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As). Organometallics 18, 4216-4221.
Weber, L., et al., 1999. Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As). Organometallics, 18(20), p 4216-4221.
L. Weber, et al., “Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As)”, Organometallics, vol. 18, 1999, pp. 4216-4221.
Weber, L., Scheffer, M.H., Stammler, H.-G., Neumann, B., Schoeller, W., Sundermann, A., Laali, K.: Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As). Organometallics. 18, 4216-4221 (1999).
Weber, Lothar, Scheffer, Matthias H., Stammler, Hans-Georg, Neumann, Beate, Schoeller, Wolfgang, Sundermann, A., and Laali, Kenneth. “Formation of Ferriophosphanyl- and Ferrioarsanyl-Functionalized Carbocation Salts by Alkylation, Protonation and Silylation of (η5-C5Me5)(CO)2FePn=C(NMe2)2 (Pn = P, As)”. Organometallics 18.20 (1999): 4216-4221.
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