Zobrazeno 1 - 10
of 12
pro vyhledávání: '"W. P. M. Nijssen"'
Autor:
Henk Stapert, Suzanne H.P.M. de Winter, Johan Lub, Jan A.M. Steenbakkers, P. C. Duineveld, Marcel Rene Bohmer, Richard J. M. Schroeders, Jeroen A. Pikkemaat, W. P. M. Nijssen
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects. 289:96-104
Micron-sized particles with a narrow size distribution are prepared by ink-jet printing technology. Droplets of a polymer solution are printed with the nozzle submerged into an aqueous phase. The particles are formed upon removal of the solvent for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e308d03eaaf102adb56f468075caa442
https://doi.org/10.1016/j.colsurfa.2006.04.011
https://doi.org/10.1016/j.colsurfa.2006.04.011
Publikováno v:
Liquid Crystals. 33:723-737
Isomerizable diacrylates derived from cinnamic acid are designed, synthesized and mixed with liquid crystalline diacrylates with the aim of making films with alternating birefringent and isotropic domains by applying the E–Z isomerization process a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72a3a9249521f95373d8cb020b6a6e36
https://doi.org/10.1080/02678290600647345
https://doi.org/10.1080/02678290600647345
Publikováno v:
Advanced Functional Materials. 15:1961-1972
This paper describes the synthesis of photoisomerizable derivatives of isosorbide. These derivatives contain a stilbene or cinnamate moiety and can therefore be used as photoisomerizable chiral compounds in cholesteric liquid-crystalline mixtures. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2439971abbc8437e2681b583195f990b
https://doi.org/10.1002/adfm.200500127
https://doi.org/10.1002/adfm.200500127
Publikováno v:
Liquid Crystals. 32:1031-1044
The syntheses of derivatives of isosorbide and cinnamic acid are described. These chiral compounds are photoisomerizable. The Z‐isomers could also be obtained after irradiation of these E‐isomeric cinnamic derivatives. The Z‐isomers were found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7055bfdf929ed3f38b4fbe263268fcca
https://doi.org/10.1080/02678290500284017
https://doi.org/10.1080/02678290500284017
Publikováno v:
Liquid Crystals. 29:995-1000
The four aldol condensation products of methylcyclohexanone isomers and 4-(4-hexyloxybenzoyloxy)benzaldehyde have been prepared. These chiral products were either obtained with high enantiomeric excess or the enantiomers were separated by means of ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::563f4b3dca79026eae15249b74527d85
https://doi.org/10.1080/02678290210143933
https://doi.org/10.1080/02678290210143933
Publikováno v:
Liquid Crystals. 29:71-77
The helical twisting powers of the E-isomers of aldol condensation products of menthone and aromatic aldehydes are higher than those of the Z-isomers. In order to find out which chiral centre of these menthone derivatives is responsible for the value
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7d8179e4b67bd03f610c54c26a6e557
https://doi.org/10.1080/02678290110086541
https://doi.org/10.1080/02678290110086541
Publikováno v:
Journal of The Electrochemical Society. 146:2397-2403
Mixtures containing liquid electrolyte and {alpha},{omega}-alkane diacrylates were produced. Upon polymerization two-phase gels consisting of polymer-rich and polymer-poor phases were obtained. The structure and the properties of the gels were studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8193423a8448232451a5d3d4d247ef7a
https://doi.org/10.1149/1.1391948
https://doi.org/10.1149/1.1391948
Autor:
A. H. Huizer, Cyril A. G. O. Varma, P. A. Kraakman, J. J. M. Vleggaar, W. P. M. Nijssen, R. J. Visser
Publikováno v:
Journal of the American Chemical Society. 116:11754-11763
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46bb1159bc76e864549486cc004b4f98
https://doi.org/10.1021/ja00105a016
https://doi.org/10.1021/ja00105a016
Autor:
Edsger C. P. Smits, R Reinder Coehoorn, Thomas D. Anthopoulos, Bert de Boer, Sepas Setayesh, Michael Buechel, Dago M. de Leeuw, W. P. M. Nijssen, Paul W. M. Blom
Publikováno v:
Advanced Materials, 19(5), 734-738. Wiley-VCH Verlag
Advanced materials, 19(5), 734-+. WILEY-V C H VERLAG GMBH
Advanced materials, 19(5), 734-+. WILEY-V C H VERLAG GMBH
Recent years have seen tremendous advances in the area of organic-based optoelectronic devices and several applications previously envisioned are now reaching the stage of commercial exploitation.[1] Organic field-effect transistors (OFETs) are among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb85884b47f03c80ef49cfe17ff11a5a
https://research.rug.nl/en/publications/77d03e55-dfc0-4a98-9b9a-8d0d77834b8e
https://research.rug.nl/en/publications/77d03e55-dfc0-4a98-9b9a-8d0d77834b8e
Publikováno v:
Advanced Materials, 15(23), 2002-2005. Wiley-VCH Verlag
A new type of semiconducting material based on polymerizable oligothiophenes (see Figure) has been prepared. In field-effect transistors, a charge-carrier mobility of 10-3 cm2 V-1 s-1 is observed prior to polymerization. Photopolymerization to a poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c9242fb96f9edff5da724285fac060d
https://research.tue.nl/nl/publications/414d831f-cdde-4a45-ac29-e4f6b17a8aa1
https://research.tue.nl/nl/publications/414d831f-cdde-4a45-ac29-e4f6b17a8aa1
