188541-09-5Relevant academic research and scientific papers
Synthesis of photosensitive organic-inorganic polymer hybrids by utilizing caged photoactivatable alkoxysilane
Ogoshi, Tomoki,Chujo, Yoshiki
, p. 5916 - 5922 (2004)
Photosensitive polymer hybrids with poly(acrylic acid) (PAA) could be obtained by using caged (photosensitive protecting group modified) alkoxysilane (NVOC-U-PTEOS). Transparent polymer hybrids were prepared with UV irradiation, while the obtained materia
Surface modification with orthogonal photosensitive silanes for sequential chemical lithography and site-selective particle deposition
Del Campo, Aranzazu,Boos, Diana,Spiess, Hans Wolfgang,Jonas, Ulrich
, p. 4707 - 4712 (2005)
(Chemical Equation Presented) Monolayer lithography: The concept of orthogonal cleavage of photolabile protecting groups was demonstrated with self-assembled silane layers on solid surfaces. Nitroveratryloxycarbonyl and benzoin derivatives can be addresse
Base-amplifying silicone resins with photobase-generating side chains and their application to negative-working photoresists
Furutani, Masahiro,Kobayashi, Hiroshi,Gunji, Takahiro,Abe, Yoshimoto,Arimitsu, Koji
, p. 1205 - 1212 (2015)
To accomplish high photosensitivity of resist systems including photobase generators, we have proposed the concept of base-proliferation reactions that generate base molecules in a nonlinear manner by the action of a catalytic amount of base; however, exc
Photolithography of self-assembled monolayers: Optimization of protecting groups by an electroanalytical method
Jennane, Jamila,Boutros, Tanya,Giasson, Richard
, p. 2509 - 2517 (1996)
Patterned surfaces presenting a high density of chemically reactive functional groups can be prepared through photolithography of self-assembled monolayers (SAM). In this paper, we report the synthesis and the evaluation of three reagents that can be used
Wavelength-selective caged surfaces: How many functional levels are possible?
San Miguel, Veronica,Bochet, Christian G.,Del Campo, Aranzazu
supporting information; scheme or table, p. 5380 - 5388 (2011/06/11)
The possibility of wavelength-selective cleavage of seven photolabile caging groups from different families has been studied. Amine-, thiol-, and carboxylic-terminated organosilanes were caged with o-nitrobenzyl (NVOC, NPPOC), benzoin (BNZ), (coumarin-4-yl)methyl (DEACM), 7-nitroindoline (DNI, BNI), and p-hydroxyphenacyl (pHP) derivatives. Caged surfaces modified with the different chromophores were prepared, and their photosensitivity at selected wavelengths was quantified. Different pairs, trios, and quartets of chromophore combinations with wavelength-selective photoresponse were identified. Our results show, for the first time, the possibility of generating surfaces with up to four different and independently addressable functional levels. In addition, this manuscript presents the first systematic comparison of the photolytic properties of different photolabile groups under different irradiation conditions.(Figure Presented)
