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Reactivity and stability of platinum(II) formyl complexes based on PCP-type ligands. The significance of sterics
Year:
2007
Source of publication :
Dalton Transactions
Authors :
Poverenov, Elena
;
.
Volume :
Co-Authors:
Vuzman, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Poverenov, E., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Diskin-Posner, Y., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Leitus, G., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Shimon, L.J.W., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Milstein, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Facilitators :
From page:
5692
To page:
5700
(
Total pages:
9
)
Abstract:
The synthesis and characterization of several Pt(ii) complexes, including formyl complexes, based on the PCP-type pincer ligands C6H 4[CH2P(iPr)2]2 (iPrPCP) and C6H4[CH2P(tBu)2]2 (tBuPCP) are described. The chloride complex (iPrPCP)PtCl (6) and the unsaturated cationic complexes [(PCP)Pt]+X- (X = OTf-, BF4-) (1, 7), based on both PCP ligands, were prepared and the latter reacted with carbon monoxide to give the corresponding cationic carbonyl complexes [(PCP)Pt(CO)]+X- (X = OTf-, BF4-) (2, 8a). Hydride nucleophilic attack on both carbonyl complexes resulted in rare neutral platinum formyl complexes (iPrPCP)Pt(CHO) (3) and (tBuPCP)Pt(CHO) (9). Complex 3 undergoes decarbonylation to the corresponding hydride complex within hours at room temperature, while the bulkier complex 9 is more stable and undergoes complete decarbonylation only after 3-4 d. This observation demonstrates the very significant steric effect of the ligand on stabilization of the corresponding formyl complexes. Reaction of complex 9 with triflic acid resulted in the carbonyl complex [(tBuPCP)Pt(CO)]+ OTf- (8b) with liberation of H2, an unusual transformation for a metal formyl. Reaction with methyl triflate resulted in the Fischer carbene-type complex, the methoxy-methylidene [(tBuPCP)Pt(CHOCH 3)]+OTf- (11). The X-ray structures of complexes 2, 6, 8a and 11 were determined. © The Royal Society of Chemistry.
Note:
Related Files :
carbon monoxide
Carbonylation
Carbonyl complex
Ligands
Platinum compounds
Room temperature
Synthesis (chemical)
Triflic acid
Show More
Related Content
More details
DOI :
10.1039/b711444c
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
18840
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:24
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Scientific Publication
Reactivity and stability of platinum(II) formyl complexes based on PCP-type ligands. The significance of sterics
Vuzman, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Poverenov, E., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Diskin-Posner, Y., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Leitus, G., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Shimon, L.J.W., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel
Milstein, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100, Israel
Reactivity and stability of platinum(II) formyl complexes based on PCP-type ligands. The significance of sterics
The synthesis and characterization of several Pt(ii) complexes, including formyl complexes, based on the PCP-type pincer ligands C6H 4[CH2P(iPr)2]2 (iPrPCP) and C6H4[CH2P(tBu)2]2 (tBuPCP) are described. The chloride complex (iPrPCP)PtCl (6) and the unsaturated cationic complexes [(PCP)Pt]+X- (X = OTf-, BF4-) (1, 7), based on both PCP ligands, were prepared and the latter reacted with carbon monoxide to give the corresponding cationic carbonyl complexes [(PCP)Pt(CO)]+X- (X = OTf-, BF4-) (2, 8a). Hydride nucleophilic attack on both carbonyl complexes resulted in rare neutral platinum formyl complexes (iPrPCP)Pt(CHO) (3) and (tBuPCP)Pt(CHO) (9). Complex 3 undergoes decarbonylation to the corresponding hydride complex within hours at room temperature, while the bulkier complex 9 is more stable and undergoes complete decarbonylation only after 3-4 d. This observation demonstrates the very significant steric effect of the ligand on stabilization of the corresponding formyl complexes. Reaction of complex 9 with triflic acid resulted in the carbonyl complex [(tBuPCP)Pt(CO)]+ OTf- (8b) with liberation of H2, an unusual transformation for a metal formyl. Reaction with methyl triflate resulted in the Fischer carbene-type complex, the methoxy-methylidene [(tBuPCP)Pt(CHOCH 3)]+OTf- (11). The X-ray structures of complexes 2, 6, 8a and 11 were determined. © The Royal Society of Chemistry.
Scientific Publication
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