SFX by Ex Libris Inc.

Title:	Synthesis of new crosslinkable co-polymers containing a push–pull zinc porphyrin for non-linear optical applications
Source:	Tetrahedron [0040-4020] Monnereau, Cyrille yr:2005

Basic

Sorry, no full text available...

Please use the document delivery service (see below)

Holding information

Holdings in library search engine ALBERT

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Plater, M. n. "A new synthetic route to donor-acceptor porphyrins." Tetrahedron 58.12 (2002): 2405-2413.
description	2.	Svenson, S. "Dendrimers in biomedical applications-reflections on the field." Advanced drug delivery reviews 57.15 (2005): 2106-29.
description	3.	Zhang, T. "Design, Synthesis, Linear, and Nonlinear Optical Properties of Conjugated (Porphinato)zinc(II)-Based Donor-Acceptor Chromophores Featuring Nitrothiophenyl and Nitrooligothiophenyl Electron-Accepting Moieties." Journal of the American Chemical Society 127.27 (2005): 9710-9720.
description	4.	Annoni, E. "Synthesis, electronic characterization and significant second-order non-linear optical responses of meso-tetraphenylporphyrins and their ZnII complexes carrying a push or pull group in the Î² pyrrolic position." European journal of inorganic chemistry 2005.19 (2005): 3857-3874.
description	5.	Subramanian, V. "Synthesis of Isocoumarins via Pd/C-Mediated Reactions of o-Iodobenzoic Acid with Terminal Alkynes." Journal of organic chemistry 70.12 (2005): 4778-8779.
description	6.	Kim, D. "A BODIPY-based reactive probe for ratiometric fluorescence sensing of mercury ions." Tetrahedron 68.26 (2012): 5279-5282.
description	7.	Bonfantini, Edia E. "Efficient synthesis of free-base 2-formyl-5, 10, 15, 20-tetraarylporphyrins, their reduction and conversion to [(porphyrin-2-yl) methyl] phosphonium salts." Journal of porphyrins and phthalocyanines 6.11/12 (2002): 708-719.
description	8.	Gillies, Elizabeth R. "Dendrimers and dendritic polymers in drug delivery." Drug discovery today 10.1 (2005): 35-43.
description	9.	Lee, Cameron C. "Designing dendrimers for biological applications." Nature biotechnology 23.12 (2005): 1517-1526.
description	10.	Astruc, D. "Dendrimers Designed for Functions: From Physical, Photophysical, and Supramolecular Properties to Applications in Sensing, Catalysis, Molecular Electronics, Photonics, and Nanomedicine." Chemical reviews 110.4 (2010): 1857-1959.
description	11.	Dennig, Jorg g. "Gene transfer into eukaryotic cells using activated polyamidoamine dendrimers." Reviews in molecular biotechnology 90.3 (2002): 339-334.
description	12.	Angiolillo, PJ. "Impact of electronic asymmetry on photoexcited triplek-state spin distributions in conjugated porphyrin oligomers probed via EPR spectroscopy." The journal of physical chemistry. B, Condensed matter, materials, surfaces, interfaces & biophysical 108.32 (2004): 11893-11903.
description	13.	Ballarin, B. "Electrochemical synthesis and characterisation of polythiophene conducting polymers functionalised by metal-containing porphyrin residue." Synthetic metals 114.3 (2000): 279-.
description	14.	Li, G. "Very stable, highly electroactive polymers of zinc(II)-5,15-bisthienylphenyl porphyrin exhibiting charge-trapping effects." Polymer 46.14 (2005): 5299-5307.
description	15.	Singh, K. "Efficient and versatile single pot approach to dipyrromethanes and bis(heterocyclyl)methanes." Tetrahedron 61.27 (2005): 6614-6622.
description	16.	Rucareanu, S. "Supramolecular assemblies between macrocyclic porphyrin hexamers and star-shaped porphyrin arrays." Journal of organic chemistry 66.15 (2001): 4973-4988.
description	17.	Gourdon, A. "Synthesis of"molecular landers"." European journal of organic chemistry 12 (1998): 2797-2801.
description	18.	Odobel, F. "Synthesis of oligothiophene-bridged bisporphyrins and study of the linkage dependence of the electronic coupling." Chemistry : a European journal 8.13 (2002): 3027-3046.
description	19.	Caminade, A. "Characterization of dendrimers." Advanced Drug Delivery Reviews 57.15 (2005): 2130-46.
description	20.	Yamamura, T. "Porphyrin Arrays Responsive to Additives. Fluorescence Tuning." Journal of the American Chemical Society 131.33 (2009): 11719-11726.