| Molecules | |
| Photophysical Properties and Kinetic Studies of 2-Vinylpyridine-Based Cycloplatinated(II) Complexes Containing Various Phosphine Ligands | |
| Reza Babadi Aghakhanpour1  Vahideh Dolatyari1  HamidR. Shahsavari1  Sareh Paziresh1  Sepideh Habibzadeh2  Mohsen Golbon Haghighi3  MohammadReza Halvagar4  | |
| [1] Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731, Iran;Department of Chemistry, Payame Noor University, Tehran P.O. BOX 19395-4697, Iran;Department of Chemistry, Shahid Beheshti University, Evin, Tehran 19839-69411, Iran;Department of Inorganic Chemistry, Chemistry and Chemical Engineering Research Center of Iran, Tehran 14968-13151, Iran; | |
| 关键词: 2-vinylpyridine; cycloplatinated(II); photophysics; kinetic; phosphine; | |
| DOI : 10.3390/molecules26072034 | |
| 来源: DOAJ | |
【 摘 要 】
A series of cycloplatinated(II) complexes with general formula of [PtMe(Vpy)(PR3)], Vpy = 2-vinylpyridine and PR3 = PPh3 (1a); PPh2Me (1b); PPhMe2 (1c), were synthesized and characterized by means of spectroscopic methods. These cycloplatinated(II) complexes were luminescent at room temperature in the yellow–orange region’s structured bands. The PPhMe2 derivative was the strongest emissive among the complexes, and the complex with PPh3 was the weakest one. Similar to many luminescent cycloplatinated(II) complexes, the emission was mainly localized on the Vpy cyclometalated ligand as the main chromophoric moiety. The present cycloplatinated(II) complexes were oxidatively reacted with MeI to yield the corresponding cycloplatinated(IV) complexes. The kinetic studies of the reaction point out to an SN2 mechanism. The complex with PPhMe2 ligand exhibited the fastest oxidative addition reaction due to the most electron-rich Pt(II) center in its structure, whereas the PPh3 derivative showed the slowest one. Interestingly, for the PPhMe2 analog, the trans isomer was stable and could be isolated as both kinetic and thermodynamic product, while the other two underwent trans to cis isomerization.
【 授权许可】
Unknown