Solution aggregation of platinum(ii) triimine methyl complexes

The NMR chemical shifts of [Pt(tpy)(CH3)](PF6) (1) and [Pt(mbzimpy)(CH3)](PF6) (2), where tpy = 2,2';6'2''-terpyridine and mbzimpy = 2,6-bis(N-methylbenzimidazol-2-yl)pyridine, in room-temperature DMSO-d6 displayed concentration dependence as a result of formation of dimers. Quan...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Dalton transactions : an international journal of inorganic chemistry Ročník 49; číslo 31; s. 10729
Hlavní autori: Shingade, Vikas M, Connick, William B
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: 11.08.2020
ISSN:1477-9234, 1477-9234
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí:The NMR chemical shifts of [Pt(tpy)(CH3)](PF6) (1) and [Pt(mbzimpy)(CH3)](PF6) (2), where tpy = 2,2';6'2''-terpyridine and mbzimpy = 2,6-bis(N-methylbenzimidazol-2-yl)pyridine, in room-temperature DMSO-d6 displayed concentration dependence as a result of formation of dimers. Quantification of these dimers, expressed by equilibrium constant (K), shows a greater tendency of 2 to aggregate in solution. Structural conformations of these dimers were confirmed by 2D 1H-1H NOESY; the results explicitly suggest a head-to-tail stacking arrangement of molecules in dimers.The NMR chemical shifts of [Pt(tpy)(CH3)](PF6) (1) and [Pt(mbzimpy)(CH3)](PF6) (2), where tpy = 2,2';6'2''-terpyridine and mbzimpy = 2,6-bis(N-methylbenzimidazol-2-yl)pyridine, in room-temperature DMSO-d6 displayed concentration dependence as a result of formation of dimers. Quantification of these dimers, expressed by equilibrium constant (K), shows a greater tendency of 2 to aggregate in solution. Structural conformations of these dimers were confirmed by 2D 1H-1H NOESY; the results explicitly suggest a head-to-tail stacking arrangement of molecules in dimers.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1477-9234
1477-9234
DOI:10.1039/d0dt02190c