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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Bochmann, Manfred Broomfield, Lewis M. Wright, Joseph A. |
| Copyright Year | 2009 |
| Abstract | The reaction of secondary phosphines HPR2 (R = Ph, Cy) with pyrrole-2-aldehydes gives a new family of 2-phosphorylmethyl-1H-pyrroles as potentially chelating mono-anionic ligands. The reaction with Ti(NMe2)4 affords octahedral Ti(NMe2)2{NC4H2(4-R′)CH2P(O)R2}2 (R′ = H, But). While the diphenylphosphoryl complexes adopt a configuration with trans-pyrrolato ligands, the dicyclohexyl analogue prefers an all-cis conformation, with profound consequences on metal–ligand bonding. The reaction of sterically undemanding HNC4H3CH2P(O)Ph2 with Y[N(SiHMe2)2]3(THF)2 give the homoleptic complex Y[NC4H3CH2P(O)Ph2]3; mixed-ligand intermediates Y[N(SiHMe2)2]2(N–O) and Y[N(SiHMe2)2](N–O)2 were identifiable but could not be isolated. The bulky ligand HNC4H2(5-But)CH2P(O)Ph2 does not react with Ti(NMe2)4 but protolyses Zn[N(SiMe3)2]2 to give a 1 : 2 complex Zn(N–O)2 as the only isolable product. On the other hand, its reaction with Y[N(SiHMe2)2]3(THF)2 affords the mono-amido complex Y{N(SiHMe2)2}{NC4H3(5-But)CH2P(O)Ph2}2 which shows good activity for the ring-opening polymerisation of cyclic esters. |
| Starting Page | 8269 |
| Ending Page | 8279 |
| Page Count | 11 |
| File Format | HTM / HTML PDF |
| ISSN | 14779226 |
| Volume Number | 0 |
| Issue Number | 39 |
| Journal | Dalton Transactions |
| DOI | 10.1039/b908394d |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Ti Pyrrole NME2 Conformational isomerism Homoleptic Ligand |
| Content Type | Text |
| Resource Type | Article |
| Subject | Inorganic Chemistry |
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