The control of chirality by optical molecular switches offers intriguing prospects in the design of new materials. For example, photochemically induced stilbene-type cis-trans isomerization of 1 (see Figure) results simultaneously in reversal of the helicity. The molecular design of switching units, the possibility of highly stereoselective optical molecular switching, and an approach to a gated response are described.</p
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
The control of chirality by optical molecular switches offers intriguing prospects in the design of ...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The control of chirality by optical molecular switches offers intriguing prospects in the design of ...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
The control of chirality by optical molecular switches offers intriguing prospects in the design of ...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
A modified version of the first generation unidirectional molecular motor showed > 99% stereosele...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The concept and the synthesis of the basic molecules for a chiroptical molecular switch are describe...
The control of chirality by optical molecular switches offers intriguing prospects in the design of ...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
Chirality in molecular opto-electronics is limited sofar to the use of optically active liquid cryst...
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