Communication: Manipulating the singlet-triplet equilibrium in organic biradical materials

被引:12
|
作者
Guenaydin-Sen, Oe. [1 ]
Fosso-Tande, J. [1 ]
Chen, P. [1 ]
White, J. L. [1 ]
Allen, T. L. [2 ]
Cherian, J.
Tokumoto, T.
Lahti, P. M. [2 ]
McGill, S. [3 ]
Harrison, R. J. [1 ,4 ]
Musfeldt, J. L. [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[3] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[4] Oak Ridge Natl Lab, Comp Sci & Math Div, Oak Ridge, TN 37831 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 135卷 / 24期
基金
美国国家科学基金会;
关键词
ELECTRONIC SPECTROSCOPY; PHOTOLYSIS; DINITRENES; SPECTRA; STATES;
D O I
10.1063/1.3672101
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We investigated the tunability of the singlet-triplet equilibrium population in the organic biradical 1,4-phenylenedinitrene via magneto-optical spectroscopy. A rich magnetochromic response occurs because applied field increases the concentration of the triplet state species, which has a unique optical signature by comparison with the singlet biradical and the precursor molecule. A Curie-like analysis of the magneto-optical properties allows us to extract the spin gap, which is smaller than previously supposed. These measurements establish the value of local-probe photophysical techniques for magnetic property determination in open-shell systems such as biradicals where a traditional electron paramagnetic resonance Curie law analysis has intrinsic limitations. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3672101]
引用
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页数:4
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