1998
DOI: 10.1039/a806802j
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4-[Di(biphenyl-4-yl)amino]azobenzene and 4,4′-bis[bis(4′-tert-butylbiphenyl-4-yl)amino]azobenzene as a novel family of photochromic amorphous molecular materials

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Cited by 75 publications
(44 citation statements)
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“…Among these, azobenzne-based photochromic amorphous molecular materials were found to exhibit trans-cis photo-isomerization reactions as amorphous films as well as in solutions [15,18]. In addition, several photomechanical effects of azobenzene-based photochromic amorphous molecular materials and crystalline materials caused by photoinduced mass transport have been found [20][21][22][23][24][25][26][27][28][29].…”
Section: Open Accessmentioning
confidence: 99%
See 1 more Smart Citation
“…Among these, azobenzne-based photochromic amorphous molecular materials were found to exhibit trans-cis photo-isomerization reactions as amorphous films as well as in solutions [15,18]. In addition, several photomechanical effects of azobenzene-based photochromic amorphous molecular materials and crystalline materials caused by photoinduced mass transport have been found [20][21][22][23][24][25][26][27][28][29].…”
Section: Open Accessmentioning
confidence: 99%
“…We have been performing studies of the creation of a low molecular-mass photochromic compound which readily form amorphous glasses, namely "photochromic amorphous molecular materials" [15][16][17][18][19]. Among these, azobenzne-based photochromic amorphous molecular materials were found to exhibit trans-cis photo-isomerization reactions as amorphous films as well as in solutions [15,18].…”
Section: Open Accessmentioning
confidence: 99%
“…Although many research focused on the low-molecular-weight AZ-doped polymers, the stability of the induced anisotropy was low. To improve stability of the recorded gratings, molecular glasses fabricated with low-molecular-weight AZ compounds were developed (Shirota et al, 1998). This kind of materials can form stable amorphous and homogenous films without scattering of visible light (Nakano et al, 2002).…”
Section: Low-molecular-weight Azsmentioning
confidence: 99%
“…Bulky ring substituents can be used to hinder the thermal back reaction. For instance, a polyurethane main-chain azo exhibited a lifetime of 4 days (thermal rate constant of k=2.8 Â 10 À6 s À1 , at 31C) (Lamarre and Sung, 1983), and an azobenzene parasubstituted with bulky pendants had a lifetime of 60 days (ko2 Â 10 À7 s À1 , at room temperature) (Shirota et al, 1998). The conformational strain of macrocylic azo compounds can also be used to lock the cis state, where lifetimes of 20 days (k=5.9 Â 10 À7 s À1 ) (Norikane et al, 2003), 1 year (half-life 400 days, k=2 Â 10 À8 s À1 ) (Rottger and Rau, 1996;Rau and Roettger, 1994), or even 6 years (k=4.9 Â 10 À9 s À1 ) (Nagamani et al, 2005) were observed.…”
mentioning
confidence: 99%