Abstract
Treatment of [MCl(CO)(PPh3)2] with K[N(R2PQ)2] afforded [M{N(Ph2PQ)2}(CO)(PPh3)] (M = Ir, Rh; Q = S, Se). The IR C=O stretching frequencies for [M(CO)(PPh3){N(Ph2PQ)2}] were found to decrease in the order S > Se. Treatment of [M(COD)Cl]2 with K[N(Ph2PQ)2] afforded [M(COD){N(Ph2PQ)2}] (COD = 1,5-cyclooctadiene; M = Ir, Rh; Q = S, Se). Treatment of [Ir(ol)2Cl] with K [ N ( Pr2i PQ )2 ] afforded [ Ir ( ol )2 { N ( Pr2i PQ )2 } ]2 (ol = cyclooctene COE, C2H4; Q = S, Se). Oxidative addition of [Ir(CO)(PPh3){N(Ph2PS)2}] and [Ir(COD){N(Ph2PS)2}] with HCl afforded [Ir(H)(Cl)(CO)(PPh3){N(Ph2PS)2}] and trans-[Ir(H)(Cl)(COD){N(Ph2PS)2}], respectively. Oxidative addition of [Ir(CO)(PPh3){N(Ph2PS)2}] with MeI afforded [Ir(Me)(I)(CO)(PPh3){N(Ph2PS)2}]. Treatment of [Ir(COE)2Cl]2 with K[N(R2PO)2] afforded [Ir(COE)2{N(Ph2PO)2}] that reacted with MeOTf (OTf = triflate) to give [Ir{N(Ph2PO)2}(COE)2(Me)(OTf)]. The crystal structures of [Ir(CO)(PPh3){N(Ph2PS)2}], [M(COD){N(Ph2PS)2}] (M = Ir, Rh), [ Ir ( ol )2 { N ( Pr2i PS )2 } ](ol = COE, C2H4), trans-[Ir(H)(Cl)(COD){N(Ph2PS)2}], and [Ir(COE)2{N(Ph2PO)2}] have been determined.
Original language | English |
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Pages (from-to) | 2712-2720 |
Number of pages | 9 |
Journal | Inorganica Chimica Acta |
Volume | 359 |
Issue number | 9 |
DOIs | |
Publication status | Published - 1 Jun 2006 |
Scopus Subject Areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry
User-Defined Keywords
- Chalcogen ligands
- Crystal structures
- Iridium
- Oxidative addition
- Rhodium