8-(Pyridin-2-yl)quinolin-7-ol and Beyond: Theoretical Design of Tautomeric Molecular Switches with Pyridine as a Proton Crane Unit DOI Creative Commons
Lidia Zaharieva, Daniela Antonová, Liudmil Antonov

et al.

Chemistry, Journal Year: 2024, Volume and Issue: 6(6), P. 1608 - 1621

Published: Dec. 6, 2024

Long-range proton transfer in several conjugated cranes, originating from 7-hydroxy quinoline as a platform, has been investigated theoretically by means of DFT and TD-DFT methodology. Major emphasis was given to their applicability provide clean switching upon irradiation. The border conditions require the existence single enol tautomer ground state, which under excitation through series consecutive exited state intramolecular steps is transferred keto tautomer. It shown that most suitable candidates are based on using iso-quinoline, pyrimidine 4-nitropyridine crane units. Their suitability function aromaticity changes, basicity nitrogen atom unit structural effects conjugation with quinoline.

Language: Английский

Azaindolizine proton cranes attached to 7-hydroxyquinoline and 3-hydroxypyridine: a comparative theoretical study DOI
Sofia O. Slavova, Liudmil Antonov

Physical Chemistry Chemical Physics, Journal Year: 2024, Volume and Issue: 26(8), P. 7177 - 7189

Published: Jan. 1, 2024

New proton cranes based on 7-hydroxy-quinoline and 3-hydroxypyridine.

Language: Английский

Citations

4

Harnessing the enol/keto-form emission of ESIPT: mechanochromism, multi-channel imaging, and detection of a chemical warfare agent mimic DOI

Kangmin Wang,

Min Zhang,

Danni Yang

et al.

Science China Materials, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 2, 2025

Language: Английский

Citations

0

Coordination-driven molecular switch on the base of an ESIPT-capable pyrimidine ligand: Synthesis, fine-tuning of emission by the halide anion and theoretical studies DOI
Nikita A. Shekhovtsov, Елена Б. Николаенкова,

S. N. Vorobyeva

et al.

Journal of Photochemistry and Photobiology A Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 116091 - 116091

Published: Oct. 1, 2024

Language: Английский

Citations

2

Theoretical Understanding of the Long-Range Proton Transfer Mechanism in 7-Hydroxy Quinoline-Based Molecular Switches: Varma’s Proton Crane and Its Analogues DOI
Sofia O. Slavova, Liudmil Antonov

The Journal of Physical Chemistry A, Journal Year: 2024, Volume and Issue: 128(7), P. 1280 - 1287

Published: Feb. 12, 2024

Herein, the detailed mechanism of intramolecular proton transfer in molecular switches, constructed from 7-hydroxy quinoline substituted eight-position C–C single axle, connected to three different cranes (morpholine, piperidine, and 1,3,5-dioxazine), was investigated by means theoretical chemistry. The interpretation rotational its stable structures were proposed for well-known Varma's crane, based on morpholine molecule. reliability simulations confirmed available literature data time-dependent IR measurements.

Language: Английский

Citations

1

Photochemistry of a proton relay – System with triple fluorescence DOI
Mihaela Avădanei, Radu Tigoianu,

Ovidiu Avadanei

et al.

Journal of Photochemistry and Photobiology A Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 116018 - 116018

Published: Sept. 1, 2024

Language: Английский

Citations

1

Tunable Emission and Structural Insights of 6-Arylvinyl-2,4-bis(2′-hydroxyphenyl)pyrimidines and Their ONO-Chelated Boron Complexes DOI Creative Commons
Rodrigo Plaza-Pedroche, M. Paz Fernández‐Liencres, Sonia B. Jiménez‐Pulido

et al.

ACS Applied Optical Materials, Journal Year: 2024, Volume and Issue: 2(10), P. 2051 - 2066

Published: Sept. 20, 2024

In this study, we present the synthesis and photophysical characteristics of a novel series 6-arylvinyl-2,4-bis(2'-hydroxyphenyl)pyrimidines. These compounds exhibit nonemissive properties attributed to potential occurrence excited-state intramolecular proton transfer process from OH groups nitrogen atoms pyrimidine ring. The introduction an acid for protonation ring results in significant enhancement fluorescence response, easily perceptible naked eye. Notably, these molecules serve as intriguing rigid O

Language: Английский

Citations

1

Stationary External Electric Field—Mimicking the Solvent Effect on the Ground-State Tautomerism and Excited-State Proton Transfer in 8-(Benzo[d]thiazol-2-yl)quinolin-7-ol DOI Creative Commons
Lidia Zaharieva, Иван Ангелов, Liudmil Antonov

et al.

Molecules, Journal Year: 2024, Volume and Issue: 29(15), P. 3506 - 3506

Published: July 26, 2024

The effect of the external electric field on ground-state tautomerism in 8-(benzo[d]thiazol-2-yl)quinolin-7-ol has been studied by using density functional theory. compound exists as an enol tautomer (off state) and under influence a long-range intramolecular proton transfer can occur, placing tautomeric at quinolyl nitrogen atom (on state). This is result much higher dipole moment end keto indicates that be used to mimic implicit solvent systems. In excited state, further stabilization most polar state leads situation when excited-state becomes impossible, limiting rotation conical intersection region.

Language: Английский

Citations

0

Strategic 1,9-Proton-Transfer-Driven Cycloaddition: Synthesis and Stereoselective Contraction of Nine-Membered Heterocycles DOI

Sekwang Baek,

Ju Young Lee,

Min Jae Kang

et al.

ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(21), P. 16105 - 16114

Published: Oct. 17, 2024

We introduce a phosphine-catalyzed cycloaddition involving unprecedented long-range intramolecular proton transfer, facilitating the synthesis of nine-membered heterocycles, which are privileged structures in natural products, as well potent pharmacophores. Experimental and computational studies revealed that enamide tether N-aromatic zwitterion directly enables regioselective transfer to proceed independently outer-sphere shuttling. This understanding selective has led improved efficiency regioselectivity desired 1,9-proton reaction under anhydrous conditions, thereby advancing development higher-order reactions. Further stereoselective contraction synthesized cyclic compounds using 3-aza-Cope rearrangement demonstrates synthetic versatility our approach. The findings this study not only advance general mechanism but also broaden its practical utility various chemical fields.

Language: Английский

Citations

0

8-(Pyridin-2-yl)quinolin-7-ol and Beyond: Theoretical Design of Tautomeric Molecular Switches with Pyridine as a Proton Crane Unit DOI Creative Commons
Lidia Zaharieva, Daniela Antonová, Liudmil Antonov

et al.

Chemistry, Journal Year: 2024, Volume and Issue: 6(6), P. 1608 - 1621

Published: Dec. 6, 2024

Long-range proton transfer in several conjugated cranes, originating from 7-hydroxy quinoline as a platform, has been investigated theoretically by means of DFT and TD-DFT methodology. Major emphasis was given to their applicability provide clean switching upon irradiation. The border conditions require the existence single enol tautomer ground state, which under excitation through series consecutive exited state intramolecular steps is transferred keto tautomer. It shown that most suitable candidates are based on using iso-quinoline, pyrimidine 4-nitropyridine crane units. Their suitability function aromaticity changes, basicity nitrogen atom unit structural effects conjugation with quinoline.

Language: Английский

Citations

0