مشخصات پژوهش

صفحه نخست /P,C-Chelation versus ...
عنوان P,C-Chelation versus P,P-coordination of unsymmetrical phosphorus ylides in palladacyclopropa[60]fullerene complexes; synthetic, spectroscopic, and theoretical studies
نوع پژوهش مقاله چاپ‌شده در مجلات علمی
کلیدواژه‌ها Phosphorus ylides, Fullerene , Synthesis, Theoretical studied
چکیده The new palladacyclopropa[60]fullerene complexes incorporating α-keto stabilized phosphorus ylides were synthesized in a three-component reaction of the unsymmetrical phosphorus ylides [Ph2P- (CH2)nPPh2vC(H)C(O)C6H4-m-R] (n = 1, R = Br, NO2, (Y1, Y2); n = 2, R = Br, NO2, (Y3, Y4)), C60 and Pd(dba)2 (dba = dibenzylideneacetone). The obtained novel P,C-chelated [(η2-C60)Pd(κ2-Y1)] (1) and [(η2-C60)Pd(κ2-Y2)] (2) complexes and P,P-coordinated [(η2-C60)Pd(Y3)2] (3) and [(η2-C60)Pd(Y4)2] (4) complexes were characterized successfully by IR, UV-Vis, ESI-MS and NMR (1H, 13C and 31P) spectroscopic methods. Complexes 1–4 are rare examples of palladacyclopropa[60]fullerene complexes with phosphorus ylide ligands. Spectroscopic results revealed that none of possible side products including P,P-coordinated [(η2-C60)Pd(Y1)2] and [(η2-C60)Pd(Y2)2] complexes and also P,C-chelated [(η2-C60)Pd(κ2-Y3)] and [(η2-C60)Pd(κ2-Y4)] complexes are formed. The EDA analysis indicated that in all the above complexes the metal–ligand bonds are mostly electrostatic in nature.
پژوهشگران سیدجواد سیدزاده صابونچی (نفر اول)، مرجان حسین زاده (نفر دوم)، علی هاشمی (نفر سوم)، صادق صالح زاده (نفر چهارم)، فرحناز ملکی (نفر پنجم)