| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1323172 | Journal of Organometallic Chemistry | 2008 | 4 Pages |
Reaction of (Ph2P(o-C6H4)CHNCH2CH2)3N with 3 equiv. of Os3(CO)10(NCMe)2 at ambient temperature affords the triple cluster [Os3(CO)10Ph2P(o-C6H4)CHNCH2CH2]3N (1) through coordination of the phosphine and imine groups. Thermolysis of 1 in benzene leads to decarbonylation and C–H/C–N bond activation of the ligand to generate (μ-H)Os3(CO)8(μ3-Ph2P(o-C6H4)CHNCCH2) (2). The molecular structure of 2 has been determined by an X-ray diffraction study.
Graphical abstractReaction of (Ph2P(o-C6H4)CHNCH2CH2)3N with 3 equiv. of Os3(CO)10(NCMe)2 affords the tripodal cluster [Os3(CO)10Ph2P(o-C6H4)CHNCH2CH2]3N (1), and thermolysis of which leads to decarbonylation and C–H/C–N bond activation of the ligand to generate (μ-H)Os3(CO)8(μ3-Ph2P(o-C6H4)CHNCCH2) (2).Figure optionsDownload full-size imageDownload as PowerPoint slide
