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Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study

[Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the o...

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Autores principales: Al Khalyfeh, Khaled, Afaneh, Akef T., Marashdeh, Ali, Almatarneh, Mansour H., Al-Mazaideh, Ghassab M., Mizyed, Shehadeh, Ashram, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542602/
https://www.ncbi.nlm.nih.gov/pubmed/33043183
http://dx.doi.org/10.1021/acsomega.0c01877
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author Al Khalyfeh, Khaled
Afaneh, Akef T.
Marashdeh, Ali
Almatarneh, Mansour H.
Al-Mazaideh, Ghassab M.
Mizyed, Shehadeh
Ashram, Muhammad
author_facet Al Khalyfeh, Khaled
Afaneh, Akef T.
Marashdeh, Ali
Almatarneh, Mansour H.
Al-Mazaideh, Ghassab M.
Mizyed, Shehadeh
Ashram, Muhammad
author_sort Al Khalyfeh, Khaled
collection PubMed
description [Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE’s and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively. Thermodynamics and stability data show that the complexes have a 1:1 ratio that has been emphasized by density functional theory calculations. Additionally, they show a synergetic interplay of donor–acceptor, π–π, and n–π interactions, which are the basis for the affinity of our novel receptors toward C(60). The proposed system of enzyme model suggests a development concept in the future design of enzyme model organic photovoltaic systems.
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spelling pubmed-75426022020-10-09 Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study Al Khalyfeh, Khaled Afaneh, Akef T. Marashdeh, Ali Almatarneh, Mansour H. Al-Mazaideh, Ghassab M. Mizyed, Shehadeh Ashram, Muhammad ACS Omega [Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE’s and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively. Thermodynamics and stability data show that the complexes have a 1:1 ratio that has been emphasized by density functional theory calculations. Additionally, they show a synergetic interplay of donor–acceptor, π–π, and n–π interactions, which are the basis for the affinity of our novel receptors toward C(60). The proposed system of enzyme model suggests a development concept in the future design of enzyme model organic photovoltaic systems. American Chemical Society 2020-09-25 /pmc/articles/PMC7542602/ /pubmed/33043183 http://dx.doi.org/10.1021/acsomega.0c01877 Text en This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Al Khalyfeh, Khaled
Afaneh, Akef T.
Marashdeh, Ali
Almatarneh, Mansour H.
Al-Mazaideh, Ghassab M.
Mizyed, Shehadeh
Ashram, Muhammad
Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title_full Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title_fullStr Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title_full_unstemmed Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title_short Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
title_sort thiacrown ethers engaged c(60) through charge transfer: experimental and theoretical study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542602/
https://www.ncbi.nlm.nih.gov/pubmed/33043183
http://dx.doi.org/10.1021/acsomega.0c01877
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