Photoswitching an Isolated Donor-Acceptor Stenhouse Adduct

被引:51
作者
Bull, James N. [1 ]
Carrascosa, Eduardo [1 ]
Mallo, Neil [2 ]
Scholz, Michael S. [1 ]
da Silva, Gabriel [3 ]
Beves, Jonathon E. [2 ]
Bieske, Evan J. [1 ]
机构
[1] Univ Melbourne, Sch Chem, Parkville, Vic 3010, Australia
[2] UNSW Sydney, Sch Chem, High St, Kensington, NSW 2052, Australia
[3] Univ Melbourne, Dept Chem Engn, Parkville, Vic 3010, Australia
基金
奥地利科学基金会; 澳大利亚研究理事会;
关键词
MOBILITY MASS-SPECTROMETRY; LIGHT RESPONSIVE POLYMER; VISIBLE-LIGHT; ION MOBILITY; PHOTOISOMERIZATION; ISOMERIZATION; PHOTOCHEMISTRY; MOLECULES; SYSTEM; PHOTO;
D O I
10.1021/acs.jpclett.7b03402
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
Donor-acceptor Stenhouse adducts (DASAs) are a new class of photoswitching molecules with excellent fatigue resistance and synthetic tunability. Here, tandem ion mobility mass spectrometry coupled with laser excitation is used to characterize the photocyclization reaction of isolated, charge-tagged DASA molecules over the 450-580 nm range. The experimental maximum response at 530 nm agrees with multireference perturbation theory calculations for the S-1 <- S-0 transition maximum at 533 nm. Photocyclization in the gas phase involves absorption of at least two photons; the first photon induces Z-E isomerization from the linear isomer to metastable intermediate isomers, while the second photon drives another E-Z isomerization and 4 pi-electrocyclization reaction. Cyclization is thermally reversible in the gas phase with collisional excitation.
引用
收藏
页码:665 / 671
页数:7
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