scholarly journals Multiple adaptation of constitutional dynamic networks and information storage in constitutional distributions of acylhydrazones

2019 ◽  
Vol 10 (1) ◽  
pp. 90-98 ◽  
Author(s):  
Guangwen Men ◽  
Jean-Marie Lehn

Acylhydrazone-based constitutional dynamic networks respond to three agents by interesting multi-adaptive behavior for processing molecular information through constituent distributions.

1991 ◽  
Vol 43 (1-2) ◽  
pp. 2853-2858 ◽  
Author(s):  
A Grupp ◽  
W Zweygart ◽  
M Mehring

2004 ◽  
Vol 69 (5) ◽  
pp. 1461-1469 ◽  
Author(s):  
Lingyun Wei ◽  
Kisari Padmaja ◽  
W. Justin Youngblood ◽  
Andrey B. Lysenko ◽  
Jonathan S. Lindsey ◽  
...  

2005 ◽  
Vol 09 (07) ◽  
pp. 491-508 ◽  
Author(s):  
Andrey B. Lysenko ◽  
Vladimir L. Malinovskii ◽  
Kisari Padmaja ◽  
Lingyun Wei ◽  
James R. Diers ◽  
...  

An approach toward molecular information storage employs redox-active molecules attached to an electroactive surface. The chief advantages of such molecular capacitors include higher charge density and more versatile synthetic design than is afforded by typical semiconductor charge-storage materials. An architecture containing two triple-decker sandwich coordination complexes and an S-acetylthiomethyl-terminated tether has been designed for multibit storage. Each triple decker is composed of two phthalocyanines, one porphyrin, and two europium atoms. The oxidation potentials of each triple decker are tuned through the use of different substituents on the phthalocyanines (t-butyl, methyl, H ) and porphyrins (pentyl, p-tolyl). Interleaving of the four cationic oxidation states of each triple decker potentially affords eight distinct oxidation states. Two dyads were examined in solution and in self-assembled monolayers (SAMs) on a Au surface. One dyad exhibited eight distinct states in solution and in the SAM, thus constituting a molecular octal counter. The potentials ranged from −0.1-+1.3 V in solution and +0.1-+1.6 V in the SAM. Taken together, this approach provides a viable means of achieving multibit information storage at relatively low potential.


2000 ◽  
Vol 65 (22) ◽  
pp. 7379-7390 ◽  
Author(s):  
Junzhong Li ◽  
Dorota Gryko ◽  
Rajeev B. Dabke ◽  
James R. Diers ◽  
David F. Bocian ◽  
...  

2004 ◽  
Vol 69 (5) ◽  
pp. 1435-1443 ◽  
Author(s):  
Arumugham Balakumar ◽  
Andrey B. Lysenko ◽  
Carole Carcel ◽  
Vladimir L. Malinovskii ◽  
Daniel T. Gryko ◽  
...  

Langmuir ◽  
2000 ◽  
Vol 16 (4) ◽  
pp. 1924-1930 ◽  
Author(s):  
Christopher L. Brown ◽  
Ulrich Jonas ◽  
Jon A. Preece ◽  
Helmut Ringsdorf ◽  
Markus Seitz ◽  
...  

ChemInform ◽  
2004 ◽  
Vol 35 (26) ◽  
Author(s):  
Lingyun Wei ◽  
Kisari Padmaja ◽  
W. Justin Youngblood ◽  
Andrey B. Lysenko ◽  
Jonathan S. Lindsey ◽  
...  

2015 ◽  
Vol 27 (10) ◽  
pp. 2035-2050 ◽  
Author(s):  
John Grogan ◽  
Rafal Bogacz ◽  
Demitra Tsivos ◽  
Alan Whone ◽  
Elizabeth Coulthard

Memory consolidation underpins adaptive behavior and dopaminergic networks may be critical for prolonged, selective information storage. To understand the time course of the dopaminergic contribution to memory consolidation in humans, here we investigate the effect of dopaminergic medication on recall and recognition in the short and longer term in Parkinson disease (PD). Fifteen people with PD were each tested on or off dopaminergic medication during learning/early consolidation (Day 1) and/or late consolidation (Day 2). Fifteen age-matched healthy participants were tested only once. On Day 1 participants learned new information, and early episodic memory was tested after 30 min. Then on Day 2, recall and recognition were retested after a 24-hr delay. Participants on medication on Day 1 recalled less information at 30 min and 24 hr. In contrast, patients on medication on Day 2 (8–24 hr after learning) recalled more information at 24 hr than those off medication. Although recognition sensitivity was unaffected by medication, response bias was dependent on dopaminergic state: Medication during learning induced a more liberal bias 24 hr later, whereas patients off medication during learning were more conservative responders 24 hr later. We use computational modeling to propose possible mechanisms for this change in response bias. In summary, dopaminergic medication in PD patients during learning impairs early consolidation of episodic memory and makes delayed responses more liberal, but enhances late memory consolidation presumably through a dopamine-dependent consolidation pathway that may be active during sleep.


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