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Author (up) Liu, R.; Azenkeng, A.; Zhouc, D.; Li, Y.; Glusac, K.D.; Sun, W. url  doi
  Title Tuning Photophysical Properties and Improving Nonlinear Absorption of Pt(II) Diimine Complexes with Extended π-Conjugation in the Acetylide Ligands Type Journal Article
  Year 2013 Publication The Journal of Physical Chemistry A Abbreviated Journal J. Phys. Chem. A  
  Volume Issue Pages 130227065352006  
  Keywords NMR FID Relaxation  
  Abstract Tuning Photophysical Properties and Improving Nonlinear Absorption of Pt(II) Diimine Complexes with Extended π-Conjugation in the Acetylide Ligands

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Rui Liu †, Alexander Azenkeng ‡, Dapeng Zhouc §, Yuhao Li †, Ksenija D. Glusac §, and Wenfang Sun *†
† Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58108-6050, United States
‡ Energy and Environmental Research Center, University of North Dakota, Grand Forks, North Dakota 58202-9018, United States
§ Department of Chemistry, Bowling Green State University, Bowling Green, Ohio 43403-0001, United States
J. Phys. Chem. A, Article ASAP
DOI: 10.1021/jp309841x
Publication Date (Web): February 11, 2013
Copyright © 2013 American Chemical Society
*E-mail: Phone: 701-231-6254. Fax: 701-231-8831.
Abstract Image

Two new Pt(II) 4,4′-di(5,9-diethyltridecan-7-yl)-2,2′-bipyridine complexes (1 and 2) bearing 9,9-diethyl-2-ethynyl-7-(2-(4-nitrophenyl)ethynyl)-9H-fluorene ligand and N-(4-(2-(9,9-diethyl-7-ethynyl-9H-fluoren-2-yl)ethynyl)phenyl)-N-phenylbenzeneamine ligand, respectively, were synthesized and characterized. Their photophysical properties were investigated systematically by UV–vis absorption, emission, and transient absorption (TA) spectroscopy, and the nonlinear absorption was studied by nonlinear transmission technique. Theoretical TD-DFT calculations using the CAM-B3LYP functional were carried out to determine the nature of the singlet excited electronic states and to assist in the assignment of significant transitions observed in experiments. Complex 1 exhibits an intense, structureless absorption band at ca. 397 nm in CH2Cl2 solution, which is attributed to mixed metal-to-ligand charge transfer (1MLCT)/ligand-to-ligand charge transfer (1LLCT)/intraligand charge transfer (1ILCT)/1π,π* transitions, and two 1MLCT/1LLCT transitions in the 300–350 nm spectral region. Complex 2 possesses an intense acetylide ligand localized 1π,π* absorption band at ca. 373 nm and a moderately intense 1MLCT/1LLCT tail above 425 nm in CH2Cl2. Both complexes are emissive in solution at room temperature, with the emitting state being tentatively assigned to the predominant 3π,π* state for 1, whereas the emitting state of 2 exhibits a switch from 3π,π* state in high-polarity solvents to 3MLCT/3LLCT state in low-polarity solvents. Both 1 and 2 exhibit strong singlet excited-state TA in the visible to NIR region, where reverse saturable absorption (RSA) is feasible. The spectroscopic studies and theoretical calculations indicate that the photophysical properties of these Pt complexes can be tuned drastically by extending the π-conjugation of the acetylide ligands. In addition, strong RSA was observed at 532 nm for nanosecond (ns) laser pulses from 1 and 2, demonstrating that the RSA of the Pt(II) diimine complexes can be improved by extending the π-conjugation of the acetylide ligands.
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  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1089-5639 ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number refbase @ admin @ Serial 13970  
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