Rubizhne Institute – a Birthplace of Photochromic Molecules DOI
Andrey G. Lvov, Daria V. Berdnikova

The Chemical Record, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 3, 2024

Abstract We introduce the community to remarkable fact that two significant discoveries in field of organic photoswitches are associated Rubizhne (Rubezhnoe) branch Research Institute Organic Intermediates and Dyes during last century. The institute was a place where researchers various nationalities carried out studies dyes for printing textiles. These efforts resulted photoswitchable hemithioindigos by M. A. Mostoslavskii peri ‐aryloxyquinones Yu. E. Gerasimenko. Herein, based on available literature, we reconstruct circumstances surrounding these outstanding findings highlight unique role as research center. Furthermore, demonstrate impact results molecules.

Language: Английский

Visible‐ and Near‐Infrared Light‐Driven Molecular Photoswitches for Biological Applications DOI Open Access
Yang Xu, Yuqi Tang, Quan Li

et al.

Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 19, 2024

Abstract Molecular photoswitches can undergo isomerization under light exposure, making them uniquely attractive for high spatiotemporal resolution remote control of biological functions. Visible and near‐infrared (NIR) light, with their low energy consumption, safety, strong tissue penetration, are particularly suitable applications. Therefore, developing visible‐ NIR light‐driven molecular use is great significance. This review introduces the most common presents state‐of‐art applications in bioimaging, biosensing, drug delivery, photocontrolled cancer phototherapy, photopharmacology. The opportunities challenges future development outlined.

Language: Английский

Citations

7

Photokinetics of Photothermal Reactions DOI Creative Commons
Mounir Maafi

Molecules, Journal Year: 2025, Volume and Issue: 30(2), P. 330 - 330

Published: Jan. 15, 2025

Photothermal reactions, involving both photochemical and thermal reaction steps, are the most abundant sequences in photochemistry. The derivation of their rate laws is standardized, but integration these has not yet been achieved. Indeed, field still lacks integrated for description reactions’ behavior and/or identification order. This made difficult a comprehensive account photokinetics photothermal which created gap knowledge. addressed present paper by introducing an unprecedented general model equation capable mapping out kinetic traces such reactions when exposed to light or dark. law also applies reactive medium either monochromatic polychromatic irradiation. validity was established against simulated data obtained fourth-order Runge–Kutta method. It then used describe quantify several situations as effects initial concentration, spectator molecules, incident radiation intensity, impact latter on photonic yield. facilitated elucidation method determine intrinsic parameters (quantum yields absorptivities species) any mechanism whose number species known. contributes rationalizing along same guidelines adopted chemical kinetics.

Language: Английский

Citations

0

Probing azobenzene-like boron nitride triazoles for their photoswitching attributes through long range push–pull effects: a DFT study DOI
Sadaf Noreen, Sajjad Hussain Sumrra, Ayesha Mohyuddin

et al.

Chemical Papers, Journal Year: 2025, Volume and Issue: unknown

Published: May 19, 2025

Language: Английский

Citations

0

Second Generation Zwitterionic Aza‐Diarylethene: Photoreversible CN Bond Formation, Three‐State Photoswitching, Thermal Energy Release, and Facile Photoinitiation of Polymerization DOI Creative Commons
Henry Dube,

Maximilian Sacherer

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 21, 2024

Abstract Diarylethenes are a well‐studied and optimized class of photoswitches with wide range applications, including data storage, smart materials, or photocontrolled catalysis biological processes. Most recently, aza‐diarylethenes have been developed in which carbon‐carbon bond connections replaced by carbon‐nitrogen connections. This structural elaboration opens up an entire new structure property space expanding the versatility applicability diarylethenes. In this work, we present second generation zwitterionic aza‐diarylethenes, finally allows for fully reversible photoswitching precise control over all three switching states. High‐yielding between neutral open form Z isomer is achieved two different wavelengths light. The third E isomeric state can be reached to 87 % upon irradiation wavelength. Its high energy content >10 kcal/mol released thermally deliberate solvent change as trigger mechanism, rendering into interesting candidates molecular solar thermal storage (MOST) applications. also serves locking state, allowing toggle light‐responsiveness reversibly labile stable switching. Further, states leads highly efficient photopolymerization methyl acrylate (MA), directly harnessing unleashed chemical reactivity our aza‐diarylethene materials application.

Language: Английский

Citations

1

Combined Photopolymerization and Localized Photochromism by Aza‐Diarylethene and Hemiindigo Synergy DOI Creative Commons

Maximilian Sacherer,

Henry Dube

Advanced Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 21, 2024

Abstract Molecular photoswitches produce light‐controlled changes at the nanometer scale and can therefore be used to alter states behavior of materials in a truly bottom‐up fashion. Here an escalating photonic complexity material property control with light is shown using recently developed aza‐diarylethene combination hemiindigo (HI) photoswitches. First, as photoswitch polystyrene (PS) reversibly inscribe relief‐type 3D structures into PS. Second, further photoinitiator for light‐induced polymerization methyl acrylate (MA), demonstrating first time chemical reactivity its zwitterionic switching state. Third, HIs are implemented polymerized MA, generating photochromic polymers. At fourth level, binary mixture allows synergize aza‐diarylethene‐induced photopolymerization localized photochromism simultaneously entrapped functional HI. With such multilevel response, utility this particular applications advanced demonstrated.

Language: Английский

Citations

1

Second Generation Zwitterionic Aza‐Diarylethene: Photoreversible CN Bond Formation, Three‐State Photoswitching, Thermal Energy Release, and Facile Photoinitiation of Polymerization DOI Creative Commons
Henry Dube,

Maximilian Sacherer

Angewandte Chemie, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 21, 2024

Abstract Diarylethenes are a well‐studied and optimized class of photoswitches with wide range applications, including data storage, smart materials, or photocontrolled catalysis biological processes. Most recently, aza‐diarylethenes have been developed in which carbon‐carbon bond connections replaced by carbon‐nitrogen connections. This structural elaboration opens up an entire new structure property space expanding the versatility applicability diarylethenes. In this work, we present second generation zwitterionic aza‐diarylethenes, finally allows for fully reversible photoswitching precise control over all three switching states. High‐yielding between neutral open form Z isomer is achieved two different wavelengths light. The third E isomeric state can be reached to 87 % upon irradiation wavelength. Its high energy content >10 kcal/mol released thermally deliberate solvent change as trigger mechanism, rendering into interesting candidates molecular solar thermal storage (MOST) applications. also serves locking state, allowing toggle light‐responsiveness reversibly labile stable switching. Further, states leads highly efficient photopolymerization methyl acrylate (MA), directly harnessing unleashed chemical reactivity our aza‐diarylethene materials application.

Language: Английский

Citations

0

Rubizhne Institute – a Birthplace of Photochromic Molecules DOI
Andrey G. Lvov, Daria V. Berdnikova

The Chemical Record, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 3, 2024

Abstract We introduce the community to remarkable fact that two significant discoveries in field of organic photoswitches are associated Rubizhne (Rubezhnoe) branch Research Institute Organic Intermediates and Dyes during last century. The institute was a place where researchers various nationalities carried out studies dyes for printing textiles. These efforts resulted photoswitchable hemithioindigos by M. A. Mostoslavskii peri ‐aryloxyquinones Yu. E. Gerasimenko. Herein, based on available literature, we reconstruct circumstances surrounding these outstanding findings highlight unique role as research center. Furthermore, demonstrate impact results molecules.

Language: Английский

Citations

0