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Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration

Authorized Users Only
2020
Authors
Milovanović, Branislav
Stanković, Ivana
Petković, Milena
Etinski, Mihajlo
Article (Published version)
,
American Chemical Society (ACS)
Metadata
Show full item record
Abstract
Guanine self-assemblies are promising supramolecular platforms for optoelectronic applications. The study (Hua et al., J. Phys. Chem. C 2012, 116, 14,682−14,689) reported that alkaline cations cannot modulate the electronic absorption spectrum of G-quadruplexes, although a cation effect is observable during electronic relaxation due to different mobility of Na+ and K+ cations. In this work, we theoretically examined whether divalent Mg2+ and Ca2+ cations and hydration might shift excited charge-transfer states of a cation-templated stacked G-quartet to the absorption red tail. Our results showed that earth alkaline cations blue-shifted nπ* states and stabilized charge-transfer ππ* states relative to those of complexes with alkaline cations, although the number of charge-separation states was not significantly modified. Earth alkaline cations were not able to considerably increase the amount of charge-transfer states below the Lb excitonic states. Hydration shifted charge-transfer s...tates of the Na+-coordinated Goctet to the absorption red tail, although this part of the spectrum was still dominated by monomer-like excitations. We found Goctet electron detachment states at low excitation energies in aqueous solution. These states were distributed over a broad range of excitation energies and could be responsible for oxidative damage observed upon UV irradiation of biological G-quadruplexes.

Keywords:
Charge-Transfer States / G-Quartet / Band structure / G-Quadruplex / Guanine / DFT / Electronic absorption spectrum / Hydration Effects / Excited states
Source:
The Journal of Physical Chemistry A, 2020, 124, 40, 8101-8111
Publisher:
  • American Chemical Society (ACS)
Funding / projects:
  • VRE for regional Interdisciplinary communities in Southeast Europe and the Eastern Mediterranean (EU-675121)
  • Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200146 (University of Belgrade, Faculty of Physical Chemistry) (RS-200146)
Note:
  • The peer-reviewed version: https://cer.ihtm.bg.ac.rs/handle/123456789/3734

DOI: 10.1021/acs.jpca.0c05022

ISSN: 1089-5639; 1520-5215

PubMed: 32936636

WoS: 000580563800001

Scopus: 2-s2.0-85092749673
[ Google Scholar ]
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URI
https://cer.ihtm.bg.ac.rs/handle/123456789/3733
Collections
  • Radovi istraživača / Researchers' publications
Institution/Community
IHTM
TY  - JOUR
AU  - Milovanović, Branislav
AU  - Stanković, Ivana
AU  - Petković, Milena
AU  - Etinski, Mihajlo
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3733
AB  - Guanine self-assemblies are promising supramolecular
platforms for optoelectronic applications. The study (Hua et al., J. Phys. Chem. C 2012, 116, 14,682−14,689) reported that alkaline cations cannot modulate the electronic absorption spectrum of G-quadruplexes, although a cation effect is observable
during electronic relaxation due to different mobility of Na+ and K+ cations. In this work, we theoretically examined whether divalent Mg2+ and Ca2+ cations and hydration might shift excited charge-transfer states of a cation-templated stacked G-quartet to the absorption red tail. Our results showed that earth alkaline cations
blue-shifted nπ* states and stabilized charge-transfer ππ* states relative to those of complexes with alkaline cations, although the number of charge-separation states was not significantly modified. Earth alkaline cations were not able to considerably increase the
amount of charge-transfer states below the Lb excitonic states. Hydration shifted charge-transfer states of the Na+-coordinated Goctet to the absorption red tail, although this part of the spectrum was still dominated by monomer-like excitations. We found Goctet electron detachment states at low excitation energies in aqueous solution. These states were distributed over a broad range of excitation energies and could be responsible for oxidative damage observed upon UV irradiation of biological G-quadruplexes.
PB  - American Chemical Society (ACS)
T2  - The Journal of Physical Chemistry A
T1  - Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration
VL  - 124
IS  - 40
SP  - 8101
EP  - 8111
DO  - 10.1021/acs.jpca.0c05022
ER  - 
@article{
author = "Milovanović, Branislav and Stanković, Ivana and Petković, Milena and Etinski, Mihajlo",
year = "2020",
abstract = "Guanine self-assemblies are promising supramolecular
platforms for optoelectronic applications. The study (Hua et al., J. Phys. Chem. C 2012, 116, 14,682−14,689) reported that alkaline cations cannot modulate the electronic absorption spectrum of G-quadruplexes, although a cation effect is observable
during electronic relaxation due to different mobility of Na+ and K+ cations. In this work, we theoretically examined whether divalent Mg2+ and Ca2+ cations and hydration might shift excited charge-transfer states of a cation-templated stacked G-quartet to the absorption red tail. Our results showed that earth alkaline cations
blue-shifted nπ* states and stabilized charge-transfer ππ* states relative to those of complexes with alkaline cations, although the number of charge-separation states was not significantly modified. Earth alkaline cations were not able to considerably increase the
amount of charge-transfer states below the Lb excitonic states. Hydration shifted charge-transfer states of the Na+-coordinated Goctet to the absorption red tail, although this part of the spectrum was still dominated by monomer-like excitations. We found Goctet electron detachment states at low excitation energies in aqueous solution. These states were distributed over a broad range of excitation energies and could be responsible for oxidative damage observed upon UV irradiation of biological G-quadruplexes.",
publisher = "American Chemical Society (ACS)",
journal = "The Journal of Physical Chemistry A",
title = "Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration",
volume = "124",
number = "40",
pages = "8101-8111",
doi = "10.1021/acs.jpca.0c05022"
}
Milovanović, B., Stanković, I., Petković, M.,& Etinski, M.. (2020). Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration. in The Journal of Physical Chemistry A
American Chemical Society (ACS)., 124(40), 8101-8111.
https://doi.org/10.1021/acs.jpca.0c05022
Milovanović B, Stanković I, Petković M, Etinski M. Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration. in The Journal of Physical Chemistry A. 2020;124(40):8101-8111.
doi:10.1021/acs.jpca.0c05022 .
Milovanović, Branislav, Stanković, Ivana, Petković, Milena, Etinski, Mihajlo, "Modulating Excited Charge-Transfer States of G‑Quartet Self- Assemblies by Earth Alkaline Cations and Hydration" in The Journal of Physical Chemistry A, 124, no. 40 (2020):8101-8111,
https://doi.org/10.1021/acs.jpca.0c05022 . .

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