Related Experiment Video
Updated: May 26, 2026

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
trans-Carbonyl-chloridobis[tris-(4-meth-oxy-phen-yl)phosphane-κP]rhodium(I)
Stefan Warsink1, Andreas Roodt
1Department of Chemistry, University of the Free State, PO Box 339, Bloemfontein 9300, South Africa.
Abstract:
The title complex, [RhCl(C(21)H(21)O(3)P)(2)(CO)], is a rhodium analogue to Vaska's complex with para-meth-oxy substituents on the six phosphan-yl-aryl units. Two independent mol-ecules are present in the unit cell, with their metal atoms both located on an inversion centre. This causes the chloride and carbonyl ligands to exhibit a positional disorder in a 0.5:0.5 ratio. The two Rh(I) atoms exhibit a distorted square-planar geometry. There are a few weak intra-molecular C-H⋯X inter-actions (X = O, Cl). Inter-estingly, no significant inter-molecular inter-actions are found between the two independent mol-ecules.
More Related Videos
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
08:46Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Related Concept Videos
Carboxylic Acids to Acid Chlorides
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism
The reaction begins with the nucleophilic addition between a phosphorus ylide and the carbonyl compound. Due to its carbanionic character, phosphorus ylide acts as a strong nucleophile and attacks the electrophilic carbonyl group. This generates a charge-separated dipolar intermediate called betaine. The negatively charged oxygen atom and...
Aldehydes and Ketones to Alkenes: Wittig Reaction Overview
Carbocations
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview