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Tmc ligand

In this paper author reported the reactivity of newly synthesized Co(III)-nitrosyls complexes with superoxide radical to follow nitric oxide dioxygenation. Two new Co(III)-nitrosyl complexes bearing N-tetramethylated cyclam (TMC) ligands, [(12-TMC)-Com(NO)]2+ (1) and [(13-TMC)Coin(NO)]2+ (2), were synthesized via [(TMC)Con(CH3CN)]2+ + NO(g) reactions. Spectroscopic and structural characterization showed that these compounds bind the nitrosyl moiety in a bent end-on fashion. Complexes 1 and 2 reacted with K02/2.2.2-ciyptand to produce [(12-TMC)Con(N02)]+ (3) and [(13-TMC)Con(N02)]+ (4), respectively these possess 0,0 -chelated nitrito ligands. [Pg.127]

Example 50 as shown in several examples trimethylchlorosilane (TMCS) acts as a highly efficient catalytic activator for the replacement of a P hjs[R2 amino group by alcohols to form the corresponding esters. Michalski and associates have noticed that compounds can also react as reagents for the replacement of a fluorine ligand by an appropriate alcohol when at least one equivalent of TMCS is used. This reaction is relatively slow. Its driving force is the formation of trimethylfluorosilane [83]. [Pg.130]

As in the case of ruthenium, a series of tra 5-dioxoosmium(VI) complexes with macrocyclic tertiary amine ligands, trans- 0 0)2(l )f (L=14-TMC, 15-TMC, 16-TMC, CRMes), have been synthesized by the method shown in Scheme 13. ... [Pg.776]

Fig. 19 Polymerization reaction of oxetane and CO2 catalyzed by (salen)CrCl and two equivalents of n-Bu4NBr at 70°C (salen ligand contains a cyclohexylene backbone for the diimine and t-butyl substituents in the 3,5-positions of the phenolates). (a) Three-dimensional infrared traces of the closely overlapped VCO2 bonds of TMC and poly(TMC). (b) Reaction profile as a function of time, where only a select number of composite infrared bands were deconvoluted... Fig. 19 Polymerization reaction of oxetane and CO2 catalyzed by (salen)CrCl and two equivalents of n-Bu4NBr at 70°C (salen ligand contains a cyclohexylene backbone for the diimine and t-butyl substituents in the 3,5-positions of the phenolates). (a) Three-dimensional infrared traces of the closely overlapped VCO2 bonds of TMC and poly(TMC). (b) Reaction profile as a function of time, where only a select number of composite infrared bands were deconvoluted...

See other pages where Tmc ligand is mentioned: [Pg.61]    [Pg.125]    [Pg.125]    [Pg.158]    [Pg.213]    [Pg.213]    [Pg.61]    [Pg.125]    [Pg.125]    [Pg.158]    [Pg.213]    [Pg.213]    [Pg.335]    [Pg.84]    [Pg.321]    [Pg.433]    [Pg.483]    [Pg.448]    [Pg.488]    [Pg.518]    [Pg.263]    [Pg.82]    [Pg.173]    [Pg.380]    [Pg.382]    [Pg.227]    [Pg.128]    [Pg.72]    [Pg.655]    [Pg.772]    [Pg.774]    [Pg.776]    [Pg.778]    [Pg.806]    [Pg.806]    [Pg.823]    [Pg.824]    [Pg.24]    [Pg.64]    [Pg.64]    [Pg.75]    [Pg.452]    [Pg.453]    [Pg.454]    [Pg.455]    [Pg.456]    [Pg.465]    [Pg.466]    [Pg.473]    [Pg.474]    [Pg.475]   
See also in sourсe #XX -- [ Pg.212 ]




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