2016
Factors influencing cyclometalations in platinum(II) complexes with tertiary phosphine ligands.
SOJKA, Martin; Jaromír TOUŠEK a Marek NEČASZákladní údaje
Originální název
Factors influencing cyclometalations in platinum(II) complexes with tertiary phosphine ligands.
Autoři
Vydání
EuCheMS Congress, Seville, Spain, 2016
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Španělsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/16:00093786
Organizační jednotka
Přírodovědecká fakulta
Klíčová slova anglicky
platinum complexes; phosphines; transition states; cyclometallation
Příznaky
Mezinárodní význam
Změněno: 2. 3. 2017 11:11, Mgr. Martin Sojka, Ph.D.
Anotace
V originále
Intramolecular activation reactions of C-H bonds on aromatic rings are frequently studied in transition metal complexes since resulting cyclometalated complexes are tested and applied in variable areas of research.[1,2] However, factors influencing proclivity of single complex for cyclometallation are far from being fully understood. We recently performed study of cyclometallations in Pt(II) complexes with phosphinoamine and phosphinophenol ligands via C-H thermal activation to evaluate the importance of ligand substitution on the reactivity of the starting compounds. The presence and positioning (ortho and para) of the substituents combined with intramolecular hydrogen interactions were found to be crucial for a successful cyclometalation. We have therefore prepared a series of organophosphorus ligands and synthesized their cis-Pt(II) complexes from PtCl2(cod). By means of 31P NMR spectroscopy we investigated their propensity for cyclometalation via thermal C-H bond activation on aromatic moieties as well as possible isomerization of cis complexes into trans isomers. We support our experimental findings by single crystal X-ray diffraction and quantum-mechanical calculations.