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Wang, Jun
Publications (3 of 3) Show all publications
Wang, J., Oruganti, B. & Durbeej, B. (2019). A Straightforward Route to Aromatic Excited States in Molecular Motors that Improves Photochemical Efficiency. ChemPhotoChem, 3(6), 450-460
Open this publication in new window or tab >>A Straightforward Route to Aromatic Excited States in Molecular Motors that Improves Photochemical Efficiency
2019 (English)In: ChemPhotoChem, ISSN 2367-0932, Vol. 3, no 6, p. 450-460Article in journal (Refereed) Published
Abstract [en]

The many successful efforts to optimize the thermal steps that are part of the reaction cycles of most light-driven rotary molecular motors have not been followed by studies providing a similarly detailed understanding of how the efficiency of the photochemical steps that actually power the motors can be improved. Against this background, we herein use computational methods to investigate the merits of an approach to increase the quantum yields of E/Z-photoisomerization-based motors by enabling one of their two moieties to become aromatic in the photoactive excited state. Through quantum chemical calculations, a straightforward route to excited states of this type is found for motors where one moiety can be transformed into an aromatic anion by an electron donor at the other moiety. Furthermore, through molecular dynamics simulations, motors operated in such excited states are indeed predicted to be much more efficient than similar motors operated in the absence of excited-state aromaticity. 

Place, publisher, year, edition, pages
Weinheim, Germany: Wiley-VCH Verlagsgesellschaft, 2019
Keywords
Aromaticity, Donor-acceptor systems, Molecular devices, Molecular dynamics, Quantum yields
National Category
Chemical Sciences
Identifiers
urn:nbn:se:liu:diva-156236 (URN)10.1002/cptc.201800268 (DOI)000471720500023 ()
Funder
Swedish Research Council, 621-2011-4353Stiftelsen Olle Engkvist Byggmästare, 2014/734 and 184-568
Note

Funding agencies:  Swedish Research Council [621-2011-4353]; Olle Engkvist Foundation [2014/734, 184-568]; Linkoping University

Available from: 2019-04-08 Created: 2019-04-08 Last updated: 2019-07-18Bibliographically approved
Zhang, J., Wang, J., Sandberg, A., Wu, X., Nyström, S., LeVine, H. I., . . . Lindgren, M. (2018). Intramolecular Proton and Charge Transfer of Pyrene-based trans-Stilbene Salicylic Acids Applied to Detection of Aggregated Proteins.. ChemPhysChem, 19(22), 3001-3009
Open this publication in new window or tab >>Intramolecular Proton and Charge Transfer of Pyrene-based trans-Stilbene Salicylic Acids Applied to Detection of Aggregated Proteins.
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2018 (English)In: ChemPhysChem, ISSN 1439-4235, E-ISSN 1439-7641, Vol. 19, no 22, p. 3001-3009Article in journal (Refereed) Published
Abstract [en]

Two analogues to the fluorescent amyloid probe 2,5-bis(4'-hydroxy-3'-carboxy-styryl)benzene (X-34) were synthesized based on the trans-stilbene pyrene scaffold (Py1SA and Py2SA). The compounds show strikingly different emission spectra when bound to preformed Aβ1-42 fibrils. This remarkable emission difference is retained when bound to amyloid fibrils of four distinct proteins, suggesting a common binding configuration for each molecule. Density functional theory calculations show that Py1SA is twisted, while Py2SA is more planar. Still, an analysis of the highest occupied molecular orbitals (HOMOs) and lowest unoccupied molecular orbitals (LUMOs) of the two compounds indicates that the degree of electronic coupling between the pyrene and salicylic acid (SA) moieties is larger in Py1SA than in Py2SA. Excited state intramolecular proton transfer (ESIPT) coupled-charge transfer (ICT) was observed for the anionic form in polar solvents. We conclude that ICT properties of trans-stilbene derivatives can be utilized for amyloid probe design with large changes in emission spectra and decay times from analogous chemical structures depending on the detailed physical nature of the binding site.less thanbr /greater than (© 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim.)

Place, publisher, year, edition, pages
Weinheim, Germany: Wiley-VCH Verlag, 2018
National Category
Theoretical Chemistry
Identifiers
urn:nbn:se:liu:diva-152767 (URN)10.1002/cphc.201800823 (DOI)000450672100006 ()30183138 (PubMedID)
Available from: 2018-11-20 Created: 2018-11-20 Last updated: 2018-12-10
Wang, J. & Durbeej, B. (2018). Toward Fast and Efficient Visible-Light-Driven Molecular Motors: A Minimal Design. ChemistryOpen, 7(8), 583-589
Open this publication in new window or tab >>Toward Fast and Efficient Visible-Light-Driven Molecular Motors: A Minimal Design
2018 (English)In: ChemistryOpen, ISSN 2191-1363, Vol. 7, no 8, p. 583-589Article in journal (Refereed) Published
Abstract [en]

A key goal in the development of light-driven rotary molecular motors is to facilitate their usage in biology and medicine by shifting the required irradiation wavelengths from the UV regime to the nondestructive visible regime. Although some progress has been made toward this goal, most available visible-light-driven motors either have relatively low quantum yields or require that thermal steps follow the photoisomerizations that underlie the rotary motion. Here, a minimal design for visible-light-driven motors without these drawbacks is presented and evaluated on the basis of state-of-the-art quantum chemical calculations and molecular dynamics simulations. The design, featuring dihydropyridinium and cyclohexenylidene motifs and comprising only five conjugated double bonds, is found to produce a full 360° rotation through fast photoisomerizations (excited-state lifetimes of ≈ 170-250 fs) powered by photons with energies well below 3 eV. 

Place, publisher, year, edition, pages
Weinheim, Germany: Wiley-VCH Verlagsgesellschaft, 2018
Keywords
isomerization, molecular devices, molecular dynamics, quantum chemistry, visible light
National Category
Chemical Sciences
Identifiers
urn:nbn:se:liu:diva-149914 (URN)10.1002/open.201800089 (DOI)30083493 (PubMedID)
Funder
Swedish Research Council, 621-2011-4353Stiftelsen Olle Engkvist Byggmästare, 2014/734 and 184-568Carl Tryggers foundation , CTS 15:134Linköpings universitet
Note

Funding agencies: Swedish Research Council [621-2011-4353]; Olle Engkvist Foundation [2014/734, 184-568]; Carl Trygger Foundation [CTS 15:134]; Linkoping University

Available from: 2018-08-03 Created: 2018-08-03 Last updated: 2018-09-13
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