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Aryl-phosphine Re complexes with SI for ChemRxiv.pdf (4.97 MB)

Determining Excited-State Structures and Photophysical Properties in Phenylphosphine Rhenium(I) Diimine Biscarbonyl Complexes Using Time-Resolved Infrared and X-ray Absorption Spectroscopies

preprint
submitted on 17.01.2021, 09:23 and posted on 19.01.2021, 04:27 by Yuushi Shimoda, Kiyoshi Miyata, Masataka Funaki, Tatsuki Morimoto, Shunsuke Nozawa, Shin-ichi Adachi, Osamu Ishitani, Ken Onda
We have explored the structural factors on the photophysical properties in two rhenium(I) diimine complexes in acetonitrile solution, cis,trans-[Re(dmb)(CO)2(PPh2Et)2]+ (Et(2,2)) and cis,trans-[Re(dmb)(CO)2(PPh3)2]+ ((3,3)) (dmb = 4,4'-dimethyl-2,2'-bipyridine, Ph = phenyl, Et = ethyl) using the combination method of time-resolved infrared spectroscopy, time-resolved extended X-ray absorption fine structure, and quantum chemical calculations. The difference between these complexes is the number of phenyl groups in the phosphine ligand, and this only indirectly affects the central Re(I). Despite this minor difference, the complexes exhibit large differences in emission wavelength and excited-state lifetime. Upon photoexcitation, the bond length of Re-P and angle of P-Re-P are significantly changed in both complexes, while the phenyl groups are largely rotated by ~20º only in (3,3). We concluded that the instability from steric effects of phenyl groups and diimine leads to the smaller Stokes shift of the lowest excited triplet state (T1) in (3,3). The large structural change between the ground and excited states causes the longer lifetime of T1 in (3,3).

History

Email Address of Submitting Author

konda@chem.kyushu-univ.jp

Institution

Kyushu University

Country

Japan

ORCID For Submitting Author

0000-0003-1724-2009

Declaration of Conflict of Interest

no conflict of interest

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