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Structure, electronic, and photophysical properties of platinum(ii) biphenyl complexes containing 2,2’-bipyridine and 1,10-phenanthroline derivatives

Platinum(II) biphenyl diimine complexes have been synthesized and characterized.
Single crystal X-ray structures from seven complexes show two types of configurations about the
platinum coordination sphere in the solid state: X and B (butterfly). The two configurations give
different circular dichroism spectra (CD) based on their C2 or Cs symmetry. The metal-to-ligand
charge transfer (MLCT) bands which occur at ~440 nm are transitions from d orbitals on the
platinum metal center to * orbitals of the diimine ligands. This agrees with the time dependant
density functional theory (TDDFT) calculations where the lowest unoccupied molecular orbitals
(LUMO) are located on diimine ligands.
Emission spectra of the complexes can be divided into three groups according to different
emission excited states: group I, ligand centered transitions (LC); group II, ligand field
transitions (LF) and group III, metal-to-ligand charge transfer (MLCT). Emission profiles from
the groups are different from one another: LC transitions have vibronic structures; LF transitions
have sharp peaks without vibronic structure and MLCT transitions have a broad peak without
vibronic structure. Linear free energy correlations were found between emission maxims,
reduction potentials and emission lifetimes with Hammett sp values. The diimine with electron
donating substituents have the higher energy emission maxima and the longer emission life time.
The diimine with electron withdrawing substituents has the lower energy emission maxima and
the shorter emission life time. / Thesis (Ph.D.)--Wichita State University, College of Liberal Arts and Sciences, Dept. of Chemistry

Identiferoai:union.ndltd.org:WICHITA/oai:soar.wichita.edu:10057/3649
Date12 1900
CreatorsHuang, Wei
ContributorsRillema, D. Paul
PublisherWichita State University
Source SetsWichita State University
Languageen_US
Detected LanguageEnglish
TypeDissertation
Formatxviii, 92 p.
RightsCopyright Wei Huang, 2010. All rights reserved

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