245326-44-7Relevant articles and documents
Rotational isomerization of (E)-(2-anthryl)ethenes. A consideration: Why are the s-cis rotamers more stable than the s-trans rotamers in the excited state and less stable in the ground state?
Karatsu, Takashi,Itoh, Hajime,Yoshikawa, Nobuko,Kitamura, Akihide,Tokumaru, Katsumi
, p. 1837 - 1849 (2007/10/03)
Rotational isomerism between s-cis and s-trans rotamers of (E)-1-(2- anthryl)-2-phenylethene (E-2APE) and (E)1-(2-anthryl)-3(3-dimethyl-1-butene (E-2ADB) were investigated by comparing the absorption, emission and transient absorption spectra with those of the model compounds. The s-trans isomer is more stable than the s-cis rotamer in the ground state; however, the s-cis isomer is more stable than the s-trans rotamer in the excited state (the lowest singlet and triplet excited state). In the triplet excited state, s-trans→s-cis one-way rotational isomerization is observed with activation energies of 30 and 18 kJ mol-1 for E-2APE and E-2ADB, respectively. Explanations of why the s-cis rotamer is more stable than the s-trans rotamer in the excited state and less stable in the ground state are proposed using the HOMO and LUMO coefficients estimated by a MOPAC93 (PM3) calculation.
