2010
DOI: 10.1016/j.cplett.2010.05.071
|View full text |Cite
|
Sign up to set email alerts
|

A photochromic thin film based on salicylideneaniline derivatives intercalated layered double hydroxide

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2013
2013
2018
2018

Publication Types

Select...
3
3

Relationship

2
4

Authors

Journals

citations
Cited by 11 publications
(3 citation statements)
references
References 31 publications
0
3
0
Order By: Relevance
“…Such behavior can be assigned to the difference between the dipole moments of trans-and cis-azobenzene isomers: the film containing the more polar cis-isomer will become more hydrophilic, while the trans-isomer makes the surface hydrophobic. Wang et al [43] have fabricated optically transparent thin films with photochromic properties by means of cointercalation of azomethine-H anions (AMH) and 1-pentanesulfonate (PS) with different molar ratios into the nanogallery of a ZnAl-LDH. XRD and SEM show that the film exhibits welldefined c-axis orientation.…”
Section: Photoinduced-responsive Materialsmentioning
confidence: 99%
“…Such behavior can be assigned to the difference between the dipole moments of trans-and cis-azobenzene isomers: the film containing the more polar cis-isomer will become more hydrophilic, while the trans-isomer makes the surface hydrophobic. Wang et al [43] have fabricated optically transparent thin films with photochromic properties by means of cointercalation of azomethine-H anions (AMH) and 1-pentanesulfonate (PS) with different molar ratios into the nanogallery of a ZnAl-LDH. XRD and SEM show that the film exhibits welldefined c-axis orientation.…”
Section: Photoinduced-responsive Materialsmentioning
confidence: 99%
“…The band located at 465 nm is due to the S 0 state of the trans-keto tautomer, and a 5 nm blue shift due to the changed weak polar microenvironment can be observed. The absence of syn-enol form indicates the inhibition of the syn-enol/anti-enol isomerization in the [174] 2D confined environment. As a result, the trans-keto tautomer of AMH is less stable in the 2D confined environment, and relaxed back isomerization is more easily to take place.…”
Section: Light-induced Sensormentioning
confidence: 97%
“…Wang et al have studied the photoisomerization process of a kind of Schiff base (azomethine-H anions, AMH) assembled LDH system [174]. Generally, after the excitation of the initial enol (anti-enol) tautomer, the excited-state intramolecular proton transfer (ESIPT) occurs for AMH, leading to the excited keto tautomer (cis-keto or its zwitterionic form), exhibiting a characteristic Stokes fluorescence band.…”
Section: Light-induced Sensormentioning
confidence: 99%