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...
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| Published in: | Dalton transactions : an international journal of inorganic chemistry Vol. 49; no. 31; p. 10729 |
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| Main Authors: | , |
| Format: | Journal Article |
| Language: | English |
| Published: |
11.08.2020
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| ISSN: | 1477-9234, 1477-9234 |
| Online Access: | Get more information |
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| Summary: | 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. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 1477-9234 1477-9234 |
| DOI: | 10.1039/d0dt02190c |