Synthesis, Air Stability, Photobleaching, and DFT Modeling of Blue Light Emitting Platinum CCC-N-Heterocyclic Carbene Pincer Complexes
Author(s) -
Xiaofei Zhang,
Ashley M. Wright,
Nathan J. DeYonker,
T. Keith Hollis,
Nathan I. Hammer,
Charles Edwin Webster,
E. Valente
Publication year - 2012
Publication title -
organometallics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.231
H-Index - 172
eISSN - 1520-6041
pISSN - 0276-7333
DOI - 10.1021/om200687w
Subject(s) - chemistry , density functional theory , excited state , carbene , pincer ligand , ligand (biochemistry) , pincer movement , metalation , time dependent density functional theory , photochemistry , transmetalation , molecular orbital , crystallography , ground state , computational chemistry , molecule , stereochemistry , atomic physics , organic chemistry , catalysis , biochemistry , receptor , physics
The recently reported metalation/transmetalation route for the synthesis of CCC-bis(NHC) pincer ligand supported transition-metal complexes was extended to Pt. 2-(1,3-Bis(N-butylimidazol-2-ylidene)phenylene)(chloro)platinum(II) (1) and its bromo analogue 2 were synthesized and characterized. X-ray crystal structure determinations revealed complexes 1 and 2 to have distorted-square-planar configurations around the metal. Photophysical and thermal properties of these complexes are reported, and their extended photostability in air is discussed and contrasted. Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) computations of the ground state and various low-lying excited states have revealed admixing of Pt 5d orbitals and the ligand π* orbitals for both the ground state and the low-lying excited states of complex 1, indicating the low-lying states to be a mixture of metal-to-ligand charge-transfer and ligand-centered transition (MLCT-LC). Somewhat surprisingly, the compute...
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