Indandiazocines: Unidirectional molecular switches
We report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-hopping trajectories for both isomerization...
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doaj-5c6c6ff425cb4c5eadbd3207873d4a422020-12-15T17:21:32ZengScienceOpenScienceOpen Research2199-10062015-01-0110.14293/S2199-1006.1.SOR-CHEM.ARDTLN.v1Indandiazocines: Unidirectional molecular switchesBernd HartkeTim RaekerWe report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-hopping trajectories for both isomerization directions, using a configuration-interaction treatment based on system-specifically reparametrized semiempirical AM1 theory. Our results are also compared to experimental and theoretical results for the parent system diazocine. We show that, as intended by design, the trans→cis bending of the azo unit in these indandiazocines can only happen in one of the two possible directions due to sterical constraints, which is a new feature for photoswitches and a necessary prerequisite for directional action at the nanoscale.https://www.scienceopen.com/document?vid=bdd94554-c0d3-4aeb-87f7-73b1bf98d860 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Bernd Hartke Tim Raeker |
spellingShingle |
Bernd Hartke Tim Raeker Indandiazocines: Unidirectional molecular switches ScienceOpen Research |
author_facet |
Bernd Hartke Tim Raeker |
author_sort |
Bernd Hartke |
title |
Indandiazocines: Unidirectional molecular switches |
title_short |
Indandiazocines: Unidirectional molecular switches |
title_full |
Indandiazocines: Unidirectional molecular switches |
title_fullStr |
Indandiazocines: Unidirectional molecular switches |
title_full_unstemmed |
Indandiazocines: Unidirectional molecular switches |
title_sort |
indandiazocines: unidirectional molecular switches |
publisher |
ScienceOpen |
series |
ScienceOpen Research |
issn |
2199-1006 |
publishDate |
2015-01-01 |
description |
We report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems
that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different
systems of this kind, we have simulated excited-state surface-hopping trajectories for both
isomerization directions, using a configuration-interaction treatment based on system-specifically
reparametrized semiempirical AM1 theory. Our results are also compared to experimental and
theoretical results for the parent system diazocine. We show that, as intended by design, the
trans→cis bending of the azo unit in these indandiazocines can only happen in one of the two
possible directions due to sterical constraints, which is a new feature for photoswitches and a necessary prerequisite for directional action at the nanoscale. |
url |
https://www.scienceopen.com/document?vid=bdd94554-c0d3-4aeb-87f7-73b1bf98d860 |
work_keys_str_mv |
AT berndhartke indandiazocinesunidirectionalmolecularswitches AT timraeker indandiazocinesunidirectionalmolecularswitches |
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1724382332876488704 |