Chelating eta(6)-arene-eta(1)-carbene ligands in ruthenium complexes
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, sa.18, ss.2862-2869, 2007 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Basım Tarihi: 2007
- Doi Numarası: 10.1002/ejic.200601189
- Dergi Adı: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Current Chemical Reactions (CCR)
- Sayfa Sayıları: ss.2862-2869
- Anahtar Kelimeler: ruthenium-arene, NHCs, imidazolinylidene, metatbesis, ROMP, polymerization, N-HETEROCYCLIC CARBENES, CLOSING OLEFIN METATHESIS, CATALYZED SUZUKI REACTION, HIGHLY-ACTIVE CATALYSTS, COUPLING REACTIONS, ARYL CHLORIDES, HETEROCARBENE LIGANDS, BISCARBENE COMPLEXES, COORDINATION CHEMISTRY, PALLADIUM COMPLEXES
- İnönü Üniversitesi Adresli: Evet
Özet
N-Heterocyclic carbene (NHC) ruthenium complexes containing a chelating NHC-eta(6)-arene ligand have been prepared and evaluated as precursors for ring opening metathesis polymerization (ROMP). The reaction of [RuCl2(p-cymene)](2) with electron-rich olefins of the bis(imidazolinylidene) type containing at least one arylmethyl-N chain (aryl: 2,4,6-trimethylphenyl, 3,4,5-trimethoxyphenyl) selectively leads, upon heating, to ruthenium(II) complexes 2 containing a chelating bridged carbene eta(6)-arene ligand. The reaction of complexes containing an additional ROCH2CH2N group with AgOTf leads to ionic complexes 5 with a tridentate trifunctional carbene/arene/ether ligand. The X-ray structure of [RuCl2{eta(1)-CN(CH2{eta 6-C6H2Me3-2,4,6})CH2CH2N(CH2-{C6H2(OMe)(3)-3,4,5})}] (2c) and that of the ionic ruthenium complex containing a trifunctional carbene/arene/ether ligand that provides ten electrons, (RuCl{eta(1)-CN(CH2{eta(6)-C6H2Me3-2,4,6})CH2CH2N(CH2CH2OCH3)}][CF3SO3] (5e), have been determined. The precursors 2 in the presence of AgOTf and propargyl alcohol, in order to produce an allenylidene initiator, and complexes 5 in the presence of propargyl alcohol lead to ROMP of norbornene. It is shown that initial chloride abstraction is required and that the catalyst activity is increased by using mesityl-ruthenium precursors and coordinated branched ether complexes. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).