1994
DOI: 10.1021/ma00099a040
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Photoresponsive Behavior of Azobenzene-Based (Meth)acrylic (Co)polymers in Thin Films

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Cited by 45 publications
(42 citation statements)
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“…In fact, several works have been reported concerning the out-of-plane alignment behavior by using unpolarized light. [114][115][116][117] From the viewpoint of 3D manipulation of molecules by light, promising results have been obtained for LCPs: by changing the incident angle of the actinic unpolarized light, one can control the alignment of AZ and mesogenic moieties in a 3D fashion, precisely along the propagation direction of the actinic light at room temperature (Figure 10 B). [ 118 ] Furthermore, it has been also confi rmed that the induced 3D alignment of molecules is very stable below T g of the LCPs.…”
Section: Photoinduced Large Change In Birefringencementioning
confidence: 99%
“…In fact, several works have been reported concerning the out-of-plane alignment behavior by using unpolarized light. [114][115][116][117] From the viewpoint of 3D manipulation of molecules by light, promising results have been obtained for LCPs: by changing the incident angle of the actinic unpolarized light, one can control the alignment of AZ and mesogenic moieties in a 3D fashion, precisely along the propagation direction of the actinic light at room temperature (Figure 10 B). [ 118 ] Furthermore, it has been also confi rmed that the induced 3D alignment of molecules is very stable below T g of the LCPs.…”
Section: Photoinduced Large Change In Birefringencementioning
confidence: 99%
“…This thermal back reaction can be enhanced by light, temperature, and solvents. 5,13,14 Transformation from Z to E was enhanced using visible light on sample 3a. From Figure 4, it was revealed that sample 3a changed its advancing contact angle from 98°to 90°(E to Z) after 15-min UV irradiation and thermal relaxation occurred within 15 min when visible light irradiation had been used.…”
Section: Photoisomerization and Wettabilitymentioning
confidence: 99%
“…The thermal back-isomerization rate was found to depend on the type of the chromophore. 5,6 The azobenzene groups without any substituents (electron-donor or electron-acceptor groups) showed relatively slower thermal Z 3 E isomerization. 6 Similar results were observed in the case of polyolefin film bearing azobenzene and the substituted azobenzene group.…”
Section: Effect Of Structure Of Chromophore On Isomerizationmentioning
confidence: 99%
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“…Side-chain azobenzene polymers have been intensively investigated [1][2][3][4][5][6][7][8] in the last decade because of their potential applications in optical storage and holographic optical elements. Their efficiency is due to the large photoinduced linear birefringence (up to 10 -2 ) assigned to the photoinduced orientation of the azobenzene moieties.…”
Section: Introductionmentioning
confidence: 99%