Room temperature synthesis of cyclometalated iridium iii complexes kinetic isomers and reactive functionalities
Yazarlar (4)
Ayan Maity
Case Western Reserve University, Amerika Birleşik Devletleri
Bryce Lane Anderson
Massachusetts Institute Of Technology, Amerika Birleşik Devletleri
Prof. Dr. Nihal DELİGÖNÜL Case Western Reserve University, Amerika Birleşik Devletleri
Thomas G. Gray
Case Western Reserve University, Amerika Birleşik Devletleri
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Chemical Science
Dergi ISSN 2041-6520 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 01-2013
Cilt / Sayı / Sayfa 4 / 3 / 1175–1181 DOI 10.1039/c2sc21831c
Makale Linki http://xlink.rsc.org/?DOI=c2sc21831c
UAK Araştırma Alanları
Anorganik Kimya
Özet
Cyclometalated iridium(III) complexes have been prepared in high yields from base-assisted transmetalation reactions of cis-bis(aquo)iridium(III) complexes with boronated aromatic proligands. Reactions proceed at room temperature. Potassium hydroxide and potassium phosphate are effective supporting bases. Kinetic, meridional isomers are isolated because of the mildness of the new technique. Syntheses are faster with KOH, but the gentler base K3PO4 broadens the reaction's scope. Complexes of chelated ketone, aldehyde, and alcohol complexes are reported that bind iridium through formally neutral oxygen and formally anionic carbon. The new complexes luminesce with microsecond-scale lifetimes at 77 K and nanosecond-scale lifetimes at room temperature; emission quenches in air. Two complexes, an aldehyde and its reduced (alcohol) derivative, are crystallographically characterized. Their bonding …
Anahtar Kelimeler
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 24
Scopus 26
Google Scholar 116
Room temperature synthesis of cyclometalated iridium iii complexes kinetic isomers and reactive functionalities

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