Magnetoelectric coupling in 4,4′-stilbenedinitrene

被引:4
|
作者
Guenaydin-Sen, Oe. [1 ]
Chen, P. [1 ]
Fosso-Tande, J. [1 ]
Allen, T. L. [2 ]
Cherian, J. [3 ]
Tokumoto, T. [3 ]
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 | 2013年 / 138卷 / 20期
基金
美国国家科学基金会;
关键词
STRUCTURE-PROPERTY RELATIONSHIPS; TRIMETHYLENEMETHANE-TYPE BIRADICALS; DENSITY-FUNCTIONAL THEORY; OPEN-SHELL MOLECULES; TRIPLET ENERGY GAPS; QUINONOIDAL DINITRENES; CONJUGATION LENGTH; BUILDING-BLOCKS; AROMATIC AZIDES; SPIN-DENSITY;
D O I
10.1063/1.4807053
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 optical properties of 4,4'-stilbenedinitrene at low temperature and in high magnetic fields and compared the results with complementary first principles calculations. Both physical tuning parameters allow us to manipulate the singlet-triplet equilibrium, and by doing so, control the optical contrast (which is on the order of -2.5x10(2) cm(-1) at 555 nm and 35 T). Moreover, analysis of the magneto-optical response using a combined population and Beer's law framework reveals the singlet-triplet spin gap and identifies particular features in the absorption difference spectrum as deriving from singlet or triplet state excitations. These findings deepen our understanding of coupling in open shell molecules and show how chemical structure modification can modulate charge-spin interactions in organic biradicals. (C) 2013 AIP Publishing LLC.
引用
收藏
页数:6
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