scholarly journals Slow Exchange of Bidentate Ligands between Rhodium(I) Complexes: Evidence of Both Neutral and Anionic Ligand Exchange

2014 ◽  
Vol 2014 (34) ◽  
pp. 5820-5826 ◽  
Author(s):  
Si Chen ◽  
Eric Manoury ◽  
Rinaldo Poli
2019 ◽  
Vol 48 (45) ◽  
pp. 16936-16942 ◽  
Author(s):  
Samuel R. Lawrence ◽  
David B. Cordes ◽  
Alexandra M. Z. Slawin ◽  
Andreas Stasch

Exchange of anionic ligands on the Mg22+ ion via an associative mechanism can be facile and depends on ligand sterics and shape.


2019 ◽  
Vol 4 (4) ◽  
pp. 819-824 ◽  
Author(s):  
Muhammad Imran ◽  
Palvasha Ijaz ◽  
Luca Goldoni ◽  
Daniela Maggioni ◽  
Urko Petralanda ◽  
...  

2006 ◽  
Vol 25 (24) ◽  
pp. 5696-5698 ◽  
Author(s):  
Kiyotaka Tanaka ◽  
Volker P. W. Böhm ◽  
David Chadwick ◽  
Michael Roeper ◽  
D. Christopher Braddock

1992 ◽  
Vol 31 (7) ◽  
pp. 1220-1223 ◽  
Author(s):  
Paul V. Bernhardt ◽  
Peter Comba ◽  
Thomas Gyr ◽  
Katalin Varnagy

2004 ◽  
Vol 43 (1) ◽  
pp. 368-374 ◽  
Author(s):  
Riccardo Vivani ◽  
Silvia Masci ◽  
Giulio Alberti

1983 ◽  
Vol 61 (8) ◽  
pp. 1800-1805 ◽  
Author(s):  
Philip A. W. Dean ◽  
Geetha K. Carson

Zn(SbF6)2 in liquid SO2 has been shown to act as an acceptor towards a variety of phosphine oxides, sulfides, and selenides, forming complexes which have been characterized in solution using 31P nmr. Slow-exchange 31P nmr spectra are reported for the complexes ZnLn2+ (n = 6, L2 = Ph2P(O)CH2P(O)Ph2 or L3 = (Ph2P(O)(CH2)2)2P(O)Ph; n = 4, L2 = Ph2P(E)CH2P(E)Ph2 (E = O, S, or Se) or bidentate (Ph2P(E)CH2)3CMe (E = S or Se), or L = (C6H11)3PE (E = O, S, or Se) or R3PE (E = S or Se, R = Ph or o-C6H4Me); n = 3, L3 = (Ph2P(E)(CH2)2)2P(E)Ph (E = S or Se) or L = R3PE (E = S or Se, R = C6H11, Ph, or o-C6H4Me); n = 2, L = R3PE (E = S or Se, R = o-C6H4Me or, perhaps, C6H11); n = 1 (possibly), L = (o-C6H4Me)3PS), and partial spectra for [Zn(SeP(C6H11)3)x(SP(C6H11)3)n−x]2+ (n = 3 or 4). No evidence was found for the mixed oxide-chalcogenide species [Zn(EP(C6H11)3)x(OP(C6H11)3)4−x]2+. In most cases the 31P nmr spectra are very similar to those reported earlier for the corresponding cadmium complexes. However, in most instances where comparison could be made it was found that the rate of intermolecular ligand exchange was less for the zinc complexes than for their cadmium counterparts. (Complexes with (Ph2P(O)(CH2)2)2P(O)Ph and Ph2P(O)(CH2)2P(O)Ph2 arc exceptional in being more labile for zinc than cadmium.)


2007 ◽  
Vol 48 (30) ◽  
pp. 5301-5303 ◽  
Author(s):  
D. Christopher Braddock ◽  
Kiyotaka Tanaka ◽  
David Chadwick ◽  
Volker P.W. Böhm ◽  
Michael Roeper

2015 ◽  
Vol 51 (18) ◽  
pp. 3870-3873 ◽  
Author(s):  
Elisa Ivry ◽  
Amos Ben-Asuly ◽  
Israel Goldberg ◽  
N. Gabriel Lemcoff

Anionic ligand exchange by amino acids readily produce chiral ruthenium benzylidenes that catalyze asymmetric olefin metathesis reactions.


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