Phosphine and Carbene Ligated Silver Acetate Easily Accessed Synthons for Reactions with Silylated Nucleophiles
 
Yazarlar (2)
Partyka David V
Creative Chemistry, Llc
Prof. Dr. Nihal DELİGÖNÜL Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Inorganic Chemistry (Q4)
Dergi ISSN 0020-1669 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 10-2009
Cilt / Sayı / Sayfa 48 / 19 / 9463–9475 DOI 10.1021/ic901371g
Makale Linki http://pubs.acs.org/doi/abs/10.1021/ic901371g
Özet
The useful synthon tricyclohexylphosphinesilver(I) acetate is easily prepared on gram scale by the reaction of silver(I) acetate and tricyclohexylphosphine in a 1:1 ratio in toluene. (PCy3)Ag(OAc) (1) reacts with a wide range of silylated nucleophiles (Me3Si-X; product with X = N3, 2; Cl, 3; SCN, 4; 1,2,4-triazol-1-yl, 5; trifluoromethanesulfonate (OTf), 6; SPh, 8; Br, 9) to effect room temperature Ag−X bond formation at the expense of the Ag−OAc bond. All new products were characterized by multinuclear NMR spectroscopies, IR spectroscopy, microanalysis, and X-ray crystallography. X-ray crystallography indicated a variety of coordination geometries at silver(I) are accessible, as di- and tetranuclear complexes were observed in all cases except 1, which forms a three-coordinate, mononuclear complex. In the case of 8, NMR and mass spectrometric data suggest fluxional species of variable nuclearity (but with empirical …
Anahtar Kelimeler
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Google Scholar 56
Scopus 4
Web of Science 47
Phosphine and Carbene Ligated Silver Acetate Easily Accessed Synthons for Reactions with Silylated Nucleophiles

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