Array Insertion and Deletion P Systems

Author(s):  
Henning Fernau ◽  
Rudolf Freund ◽  
Sergiu Ivanov ◽  
Markus L. Schmid ◽  
K. G. Subramanian
2011 ◽  
Vol 110 (1-4) ◽  
pp. 13-28 ◽  
Author(s):  
Artiom Alhazov ◽  
Alexander Krassovitskiy ◽  
Yurii Rogozhin ◽  
Sergey Verlan

Author(s):  
Artiom Alhazov ◽  
Alexander Krassovitskiy ◽  
Yurii Rogozhin

2013 ◽  
Vol 128 ◽  
pp. 62-75 ◽  
Author(s):  
Rudolf Freund ◽  
Sergiu Ivanov ◽  
Marion Oswald ◽  
K.G. Subramanian

2014 ◽  
Vol 13 (2) ◽  
pp. 257-268 ◽  
Author(s):  
Rudolf Freund ◽  
Yurii Rogozhin ◽  
Sergey Verlan

2009 ◽  
Vol 1 ◽  
pp. 108-117 ◽  
Author(s):  
Alexander Krassovitskiy ◽  
Yurii Rogozhin ◽  
Sergey Verlan

2011 ◽  
Vol 412 (1-2) ◽  
pp. 136-144 ◽  
Author(s):  
Artiom Alhazov ◽  
Alexander Krassovitskiy ◽  
Yurii Rogozhin ◽  
Sergey Verlan

2019 ◽  
Author(s):  
Terri Lovell ◽  
Curtis Colwell ◽  
Lev N. Zakharov ◽  
Ramesh Jasti

<p>[<i>n</i>]Cycloparaphenylenes, or “carbon nanohoops,” are unique conjugated macrocycles with radially oriented p-systems similar to those in carbon nanotubes. The centrosymmetric nature and conformational rigidity of these molecules lead to unusual size-dependent photophysical characteristics. To investigate these effects further and expand the family of possible structures, a new class of related carbon nanohoops with broken symmetry is disclosed. In these structures, referred to as <i>meta</i>[<i>n</i>]cycloparaphenylenes, a single carbon-carbon bond is shifted by one position in order to break the centrosymmetric nature of the parent [<i>n</i>]cycloparaphenylenes. Advantageously, the symmetry breaking leads to bright emission in the smaller nanohoops, which are typically non-fluorescent due to optical selection rules. Moreover, this simple structural manipulation retains one of the most unique features of the nanohoop structures-size dependent emissive properties with relatively large extinction coefficents and quantum yields. Inspired by earlier theoretical work by Tretiak and co-workers, this joint synthetic, photophysical, and theoretical study provides further design principles to manipulate the optical properties of this growing class of molecules with radially oriented p-systems.</p>


2019 ◽  
Author(s):  
Terri Lovell ◽  
Curtis Colwell ◽  
Lev N. Zakharov ◽  
Ramesh Jasti

<p>[<i>n</i>]Cycloparaphenylenes, or “carbon nanohoops,” are unique conjugated macrocycles with radially oriented p-systems similar to those in carbon nanotubes. The centrosymmetric nature and conformational rigidity of these molecules lead to unusual size-dependent photophysical characteristics. To investigate these effects further and expand the family of possible structures, a new class of related carbon nanohoops with broken symmetry is disclosed. In these structures, referred to as <i>meta</i>[<i>n</i>]cycloparaphenylenes, a single carbon-carbon bond is shifted by one position in order to break the centrosymmetric nature of the parent [<i>n</i>]cycloparaphenylenes. Advantageously, the symmetry breaking leads to bright emission in the smaller nanohoops, which are typically non-fluorescent due to optical selection rules. Moreover, this simple structural manipulation retains one of the most unique features of the nanohoop structures-size dependent emissive properties with relatively large extinction coefficents and quantum yields. Inspired by earlier theoretical work by Tretiak and co-workers, this joint synthetic, photophysical, and theoretical study provides further design principles to manipulate the optical properties of this growing class of molecules with radially oriented p-systems.</p>


Sign in / Sign up

Export Citation Format

Share Document