2013
DOI: 10.1039/c3ra45130e
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An i-line molecular glass photoresist for high resolution patterning

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Cited by 3 publications
(2 citation statements)
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“…S18 (ESI †), the sharp and strong peaks of Cz-CSN-OH revealed its high crystallinity, and the broad and weak signals of HSMGs demonstrated their amorphous states. The amorphous nature of HSMGs are caused by the asymmetric structure of CRA derivatives containing bulky substituent groups, [26,45] which represented that the introduction of NLO chromophores into CRA core molecule could effectively avoid the crystallization of NLO chromophores. The amorphous states of HSMGs are helpful to improving their PR properties.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
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“…S18 (ESI †), the sharp and strong peaks of Cz-CSN-OH revealed its high crystallinity, and the broad and weak signals of HSMGs demonstrated their amorphous states. The amorphous nature of HSMGs are caused by the asymmetric structure of CRA derivatives containing bulky substituent groups, [26,45] which represented that the introduction of NLO chromophores into CRA core molecule could effectively avoid the crystallization of NLO chromophores. The amorphous states of HSMGs are helpful to improving their PR properties.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…In addition, as the NLO chromophore was synthesized in advance, the problem that two acceptors were introduced into the 3, 6-position of carbazole caused by post-functionalization could be completely avoided. Furthermore, the rigid 3D CRA core was helpful for maintaining the amorphous state in HSMGs at room temperature [11,26] and decreasing the NLO chromophores antiparallel packing. According to the previous work, [27,28] the methine NLO chromophore, with carbazole as donor and a nitrobenzene and a cyano group as acceptor (Cz-CSN-OH, Scheme 1), was chosen to construct HSMGs firstly, due to its better PR performance than the other chromophores.…”
Section: Introductionmentioning
confidence: 99%