scholarly journals Controlling Contact Configuration of Carboxylic Acid-Based Molecular Junctions Through Side Group

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Jun-Ren Huang ◽  
Hong Huang ◽  
Cai-Ping Tao ◽  
Ju-Fang Zheng ◽  
Ying Yuan ◽  
...  
2017 ◽  
Vol 19 (46) ◽  
pp. 31345-31351 ◽  
Author(s):  
Juan Ramón Avilés-Moreno ◽  
Giel Berden ◽  
Jos Oomens ◽  
Bruno Martínez-Haya

Protonated arginine interacts with 12-crown-4 through the guanidinium side group. In the complex with the N-substituted analog cyclen, the dominant conformation is the result of the proton transfer from the carboxylic acid group of the amino acid to the macrocycle.


2017 ◽  
Vol 56 (48) ◽  
pp. 15378-15382 ◽  
Author(s):  
Ali Khalid Ismael ◽  
Kun Wang ◽  
Andrea Vezzoli ◽  
Mohsin K. Al-Khaykanee ◽  
Harry E. Gallagher ◽  
...  

2017 ◽  
Vol 129 (48) ◽  
pp. 15580-15584 ◽  
Author(s):  
Ali Khalid Ismael ◽  
Kun Wang ◽  
Andrea Vezzoli ◽  
Mohsin K. Al-Khaykanee ◽  
Harry E. Gallagher ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Saeideh Ramezani Akbarabadi ◽  
Mojtaba Madadi Asl

Transport properties of molecular junctions are prone to chemical or conformational modifications. Perturbation of the molecule-electrode coupling with anchoring groups or functionalization of the molecule with side groups is a well-characterized method to modulate the thermoelectric properties of molecular junctions. In this study, we used wide-band approximation combined with the non-equilibrium Green’s function (NEGF) formalism to inspect conductance, thermopower and figure of merit of an anthracene molecule coupled to gold (Au) electrodes. To provide a comparative study, three different anchoring groups were used, i.e., thiol, isocyanide and cyanide. The molecule was then perturbed with the amine side group in two positions to explore the interplay between anchoring groups and the side group. We showed that the introduction of side group alters transmission probability near the Fermi energy where transmission peaks are shifted relative to the Fermi level compared to the unperturbed molecule (i.e., without side group), ultimately leading to modified electrical and thermoelectric properties. The greatest value of electrical conductance was achieved when the side-group-perturbed molecule was anchored with isocyanide, whereas the thiol-terminated molecule perturbed with the side group yielded the greatest value of thermal conductance. We found that the Wiedemann-Franz law is violated in the Au-anthracene-Au device. Furthermore, the highest thermopower and figure of merit were attained in the cyanide-terminated perturbed molecule. Our results indicate that charge donating/accepting character of the anchoring group and its interplay with the side group position can modify temperature dependency of conductance, thermopower and figure of merit which is in agreement with experimental findings in organic molecular junctions. Such modifications may potentially contribute to the understanding of emerging conductance-based memory devices designed to mimic the behavior of brain-like synapses.


Micromachines ◽  
2018 ◽  
Vol 9 (5) ◽  
pp. 234 ◽  
Author(s):  
Miao-Ling Huang ◽  
Fan Zhang ◽  
Chen Wang ◽  
Ju-Fang Zheng ◽  
Hui-Ling Mao ◽  
...  

1993 ◽  
Vol 3 (6) ◽  
pp. 865-889 ◽  
Author(s):  
Norbert Schwenk ◽  
Hans Wolfgang Spiess
Keyword(s):  

1969 ◽  
Vol 21 (02) ◽  
pp. 294-303 ◽  
Author(s):  
H Mihara ◽  
T Fujii ◽  
S Okamoto

SummaryBlood was injected into the brains of dogs to produce artificial haematomas, and paraffin injected to produce intracerebral paraffin masses. Cerebrospinal fluid (CSF) and peripheral blood samples were withdrawn at regular intervals and their fibrinolytic activities estimated by the fibrin plate method. Trans-form aminomethylcyclohexane-carboxylic acid (t-AMCHA) was administered to some individuals. Genera] relationships were found between changes in CSF fibrinolytic activity, area of tissue damage and survival time. t-AMCHA was clearly beneficial to those animals given a programme of administration. Tissue activator was extracted from the brain tissue after death or sacrifice for haematoma examination. The possible role of tissue activator in relation to haematoma development, and clinical implications of the results, are discussed.


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