Photoswitching hydrazones based on benzoylpyridine. Issue 44 (4th November 2019)
- Record Type:
- Journal Article
- Title:
- Photoswitching hydrazones based on benzoylpyridine. Issue 44 (4th November 2019)
- Main Title:
- Photoswitching hydrazones based on benzoylpyridine
- Authors:
- Mravec, Bernard
Filo, Juraj
Csicsai, Klaudia
Garaj, Vladimír
Kemka, Miroslav
Marini, Anna
Mantero, Mariachiara
Bianco, Andrea
Cigáň, Marek - Abstract:
- Abstract : The photoswitching behaviour of three readily accesible benzoylpyridine hydrazones, whose photochromic properties depend on the benzoyl substituent and intermolecular interactions, was investigated. Abstract : The photoswitching properties of three readily accesible benzoylpyridine hydrazones were investigated. Interestingly, replacing classical stirring with ultrasound wave activation results in pure thermodynamically less stable E isomer crystallization at room temperature. The studied benzoylpyridine hydrazones exhibit both P- and T-photochromic behaviour, depending on the benzoyl substituent, and improved addressability compared to most of the previously published pyridyl based hydrazones and 2-pyridylcarboxaldehyde acylhydrazones. Low activation entropy and calculated transition state geometry favour the inversion mechanism of their thermal isomerization rather than tautomerization followed by rotation recently found for pyridyl-hydrazone ester or nitrile rotary switches. The association behaviour of the nitro derivative during its thermal E -to- Z isomerization in highly polar DMSO indicates an important role of intermolecular hydrogen bonding in the thermal kinetics of benzoylpyridine-based hydrazone photoswitches. Moreover, the addition of triethylamine significantly accelerates the rate of Z -isomer thermal isomerization from days to seconds and could thus pave the way to fast pyridyl hydrazone T-type photochromic compounds in polar solvents. This studyAbstract : The photoswitching behaviour of three readily accesible benzoylpyridine hydrazones, whose photochromic properties depend on the benzoyl substituent and intermolecular interactions, was investigated. Abstract : The photoswitching properties of three readily accesible benzoylpyridine hydrazones were investigated. Interestingly, replacing classical stirring with ultrasound wave activation results in pure thermodynamically less stable E isomer crystallization at room temperature. The studied benzoylpyridine hydrazones exhibit both P- and T-photochromic behaviour, depending on the benzoyl substituent, and improved addressability compared to most of the previously published pyridyl based hydrazones and 2-pyridylcarboxaldehyde acylhydrazones. Low activation entropy and calculated transition state geometry favour the inversion mechanism of their thermal isomerization rather than tautomerization followed by rotation recently found for pyridyl-hydrazone ester or nitrile rotary switches. The association behaviour of the nitro derivative during its thermal E -to- Z isomerization in highly polar DMSO indicates an important role of intermolecular hydrogen bonding in the thermal kinetics of benzoylpyridine-based hydrazone photoswitches. Moreover, the addition of triethylamine significantly accelerates the rate of Z -isomer thermal isomerization from days to seconds and could thus pave the way to fast pyridyl hydrazone T-type photochromic compounds in polar solvents. This study could therefore contribute to general knowledge related to the photochromic behaviour of hydrazones as an important class of modern photoswitches. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 44(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 44(2019)
- Issue Display:
- Volume 21, Issue 44 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 44
- Issue Sort Value:
- 2019-0021-0044-0000
- Page Start:
- 24749
- Page End:
- 24757
- Publication Date:
- 2019-11-04
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cp05049c ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12279.xml