Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marijana Fazekas"'
Autor:
Mathias O. Senge, Frances Blaikie, Monica Pintea, Aoife M. Ryan, Romain Perusitti, Andreas Gehrold, Marijana Fazekas, Oliver B. Locos
Publikováno v:
European Journal of Organic Chemistry. 2011:5817-5844
Current applications of porphyrins in medicine and optics, such as photodynamic therapy or nonlinear absorbers, increasingly require the use of far-red absorbing dyes. Modifications of the porphyrin structure to accommodate these conditions can be ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b0ff08bf7554a3781b38eae3f15222b
https://doi.org/10.1002/ejoc.201100642
https://doi.org/10.1002/ejoc.201100642
Publikováno v:
European Journal of Organic Chemistry. 2011:5797-5816
Development of efficient new synthetic strategies leading to more diversified substitution patterns of porphyrin rings is of great importance as it expands the potential applicability of these compounds and provides a more accurate way of tailoring t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b46c3a20fbf778370c7e63c4a11df614
https://doi.org/10.1002/ejoc.201100641
https://doi.org/10.1002/ejoc.201100641
Autor:
Flavia Popa, Pedro Lameiras, Mircea Darabantu, Camelia Berghian, Ioan Silaghi-Dumitrescu, Constantin Bele, Nelly Plé, Ionut Cadis, Marijana Fazekas, Monica Pintea
Publikováno v:
Tetrahedron. 64:8851-8870
The iterative synthesis of 2,4,6-triamino-s-triazines (melamines), precursors and dendritic structures, by amination of cyanuric chloride with C-1 versus C-2-substituted 2-aminopropane-1,3-diols (serinols), is comparatively examined. The stereochemis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1767f965ace0161aaa585759bfcbef35
https://doi.org/10.1016/j.tet.2008.06.071
https://doi.org/10.1016/j.tet.2008.06.071
Autor:
E. M. Ni Mhuircheartaigh, Mathias O. Senge, Marijana Fazekas, Monika Zawadzka, E. G. A. Notaras, Oliver B. Locos, Werner J. Blau
Publikováno v:
Advanced Materials. 19:2737-2774
Porphyrins and phthalocyanines have outstanding chemical and thermal stability. The macrocyclic structure and chemical reactivity of tetrapyrroles offers architectural flexibility and facilitates the tailoring of chemical, physical and optoelectronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5508f2ba646ae6f51a2646ba287038d
https://doi.org/10.1002/adma.200601850
https://doi.org/10.1002/adma.200601850
Autor:
Ioan Silaghi-Dumitrescu, Alain Turck, Monica Pintea, Camelia Berghian, Pedro Lameiras, Mircea Darabantu, Isabelle Delhom, Nelly Plé, Marijana Fazekas
Publikováno v:
Letters in Organic Chemistry. 3:905-910
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e67b2ce0c41f28250bf769513b21cb34
https://doi.org/10.2174/157017806779467933
https://doi.org/10.2174/157017806779467933
Publikováno v:
European Journal of Organic Chemistry. 2011
The cover picture shows the meso functionalization of 5,10- and 5,15-A2-porphyrins by using a conveyor belt, whereby the porphyrin is functionalized with various substituents (different coloured boxes) and various linkers. When these functionalized p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d4a91e832478d64edda9635305b8327
https://doi.org/10.1002/ejoc.201190082
https://doi.org/10.1002/ejoc.201190082
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(48)
Current applications in porphyrin chemistry require the use of unsymmetrically substituted porphyrins. Many current industrial interests in optics and biomedicine require systems with either push-pull (electron-donating and -withdrawing groups) or am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6cc0a9dfbfefc81dfe2ea49541b03b
https://pubmed.ncbi.nlm.nih.gov/22038942
https://pubmed.ncbi.nlm.nih.gov/22038942
Publikováno v:
Chemical communications (Cambridge, England). (21)
A(2)B(2)-type push-pull porphyrins with a strong intramolecular dipole moment have been prepared via Heck and Suzuki coupling reactions as novel materials for use in nonlinear optics (NLO); they display saturable (SA) and reverse saturable absorption
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ab1ab4748eca786d8ce42fed2850391
https://pubmed.ncbi.nlm.nih.gov/17520124
https://pubmed.ncbi.nlm.nih.gov/17520124
Autor:
Monica Pintea, Nelly Plé, Pedro Lameiras, Mircea Darabantu, Isabelle Delhom, Marijana Fazekas, Camelia Berghian, Constantin Bele
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b69cb4146bd061ba1df3e94d31e06437
https://doi.org/10.1515/hc.2006.12.2.135
https://doi.org/10.1515/hc.2006.12.2.135
Autor:
Camelia Berghian, Monica Pintea, Marijana Fazekas, Nelly Plé, Pedro Lameiras, Mircea Darabantu, Constantin Bele
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10cc0eae332e01f98f199f28283ea07a
https://doi.org/10.1515/hc.2006.12.2.151
https://doi.org/10.1515/hc.2006.12.2.151