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Показана возможность ихиспользования в качестве катализаторов жидкофазного фотоокисления антрацена.5.Исследованы свойства сферических аморфных наночастиц (CАНЧ) из смеситритерпеноидов бересты (СТБ), функционализированных амфифильными порфиринами.Полученные наночастицы являются стабильными в физиологических условиях, обладаютразмерами в диапазоне 100–200 нм и могут найти применение в качестве нанопрепаратовдля ФДТ.1406. Список литературы1.Biju, V. Chemical modifications and bioconjugate reactions of nanomaterials forsensing, imaging, drug delivery and therapy / V.
Biju // Chem. Soc. Rev. –2014. –Vol. 43, №3. –P. 744–764.2.Umeyama, T. Photofunctional Hybrid Nanocarbon Materials / T. Umeyama, H.Imahori // J. Phys. Chem. C. –2013. –Vol.117, № 7. –P. 3195–3209.3.Sanchez, C. Molecular Engineering of Functional Inorganic and Hybrid Materials/ Sanchez C., Boissiere C., Cassaignon S., Chaneac C., Durupthy O., Faustini M., Grosso D.,Laberty-Robert C., Nicole L., Portehault D., Ribot F., Rozes L., Sassoye C.
// Chem. Mater. –2014. –Vol.26, №1. –P. 221–238.4.Ishihara, S. Porphyrin-based sensor nanoarchitectonics in diverse physicaldetection modes / Ishihara S., Labuta J., Rossom W. V., D. Ishikawa, Minami K., Hill J. P.,Ariga K. // Phys. Chem. Chem. Phys. –2014. –Vol. 16. – Р.
9713–9746.5.Mojzisova, H. Structural and physico-chemical determinants of the interactionsof macrocyclic photosensitizers with cells / Mojzisova H., Bonneau S., Brault D. // Eur. Biophys.J. –2007. –Vol.36, №8. –P.943–953.6.Soloway, A. H. The Chemistry of Neutron Capture Therapy / Soloway A. H.,Tjarks W., Barnum B. A., Rong F.-G., Barth R. F., Codogni I. M., Wilson J. G. // Chem. Rev. –1998. –Vol.
98, № 4. –P.1515–15627.Senge, M. O. Nonlinear Optical Properties of Porphyrins / Senge M. O., FazekasM., Notaras E. G. A., Blau W. J., Zawadzka M., Locos O. B., Mhuircheartaigh E. M. N. // Adv.Mater. –2007. –Vol. 19. –P. 2737–2774.8.Wu, J. Dynamic [2] Catenanes Based on a Hydrogen Bonding-Mediated Bis-ZincPorphyrin Foldamer Tweezer: A Case Study / Wu J., Fang F., Lu W.-Y., Hou J.-L., Li C., WuZ.-Q., Jiang X.-K., Li Z.-T., Yu Y.-H.
// J. Org. Chem. –2007. –Vol. 72, № 8. –P. 2897–2905.9.Sanchez, C. Applications of advanced hybrid organic-inorganic nanomaterials:from laboratory to market / Sanchez C., Belleville P., Popall M., Nicole L. // Chem. Soc. Rev . –2011. –Vol.40. –P. 696–753.10.Wang, H. Strongly coupled inorganic–nano-carbon hybrid materials for energystorage / Wang H., Dai H. // Chem.
Soc. Rev. –2013. –Vol.42, –3088–3113.11.Pagona, G. Carbon Nanohorn–Porphyrin Dimer Hybrid Material for EnhancingLight-Energy Conversion /Pagona G., Zervaki G.E., Sandanayaka A. S. D., Ito O.,141Charalambidis G., Hasobe T., Coutsolelos A. G., Tagmatarchis N. // J. Phys. Chem. C, –2012. –Vol.116, № 17. –P. 9439–9449.12.Carvalho, C.
M. B.Functional Cationic Nanomagnet−Porphyrin Hybrids for thePhotoinactivation of Microorganisms / Carvalho C. M. B., Alves E., Costa L., Tom éJ. P. C.,Faustino M. A. F., Neves M. G. P. M. S., Tom é A. C., Cavaleiro J. A. S., Almeida A., CunhaÂ., Lin Z., Rocha J. // ACS Nano. –2010. –Vol. 4, № 12. –P.
7133–7140.13.Said, A. J.Hybrid Bulk Heterojunction Solar Cells Based on P3HT and Porphyrin-Modified ZnO Nanorods / Said A. J., Poize G., Martini C., Ferry D., Marine W., Giorgio S.,Fages F., Hocq J., Boucle J., Nelson J., Durrant J. R., Ackermann J. // J. Phys. Chem. C. –2010.–Vol. 114, № 25. –P. 11273–11278.14.Ozawa, H.Supramolecular Hybrid of Gold Nanoparticles and SemiconductingSingle-Walled Carbon Nanotubes Wrapped by a Porphyrin–Fluorene Copolymer / Ozawa H., YiX., Fujigaya T., Niidome Y., Asano T., Nakashima N. // J.
Am. Chem. Soc. –2011. –Vol. 133, №37. –P. 14771–14777.15.Семейкин, А.С. Синтез и физико-химические свойства синтетическихпорфиринов в неводных растворах: дис. на соиск. учен. степ. докт. хим. наук (02.00.03)/Семейкин Александр Станиславович; Институт химии неводных растворов РАН. –Иваново, 1995. С.67.16.Treibs, F. Über die Synthese und die Elektronenspektren ms-substituierterPorphine / Treibs F., Haberle H., Liebigs J. // Ann. Chem .
–1968. –Vol. 718, № 1. –P. 183–207.17.Kruper, W. J. Regiospecific aryl nitration of meso-substituted tetraarylporphyrins:a simple route to bifunctional porphyrins / Kruper W. J., Chamberlin A. T., Kochanny M. J. //Org. Chem. –1989. –Vol. 54, №11. –Р. 2753–2756.18.Meng, G.G. Porphyrin chemistry pertaining to the design of anti-cancer drugs;part 1, the synthesis of porphyrins containingmeso-pyridyl and meso-substituted phenylfunctional groups / Meng G.G., James B.R., Skov K.A. // Can. J.
Chem. –1994. –Vol.72, № 9. –P. 1894–1909.19.Luguya, R. Synthesis and reactions ofmeso-(p-nitrophenyl)porphyrins / LuguyaR., Jaquinod L., Fronczek F. R., M. Vicente M.G., Smith K.M. // Tetrahedron. –2004. –Vol.60,№ 12. –P. 2757–2763.20.Collman, J.P. Reversible oxygen adduct formation in ferrous complexes derivedfrom a picket fence porphyrin. Model for oxymyoglobin / Collman J.P., Gagne R.R., HalbertT.R.,Marchon J.C., Reed C.A.
// J. Amer. Chem. Soc. –1973. –Vol.95, № 23.–P. 7868–7870.14221.КолодинаЕ.А.Реакционнаяспособностьмезо-фенилзамещенныхпорфиринов в реакции нитрования: автореф. дис. на соиск. учен. степ. канд. хим. Наук(02.00.03) / Колодина Екатерина Александровна; Ивановский государственный химикотехнологический университет. –Иваново, 2010. – 5 с.22.Adler, A. D.
A simplified synthesis for meso-tetraphenylporphine / Adler A. D.,Longo F. R., Finarelli J. D., Goldmacher J., Assour J., Korsakoff L. //J. Org. Chem . –1967. –Vol.32, № 2. –P. 476–476.23.Sun, Z. Synthesis of p-substituted tetraphenylporphyrins andcorresponding ferriccomplexes with mixed-solvents method / Sun Z., She Y., Zhong R.
// Front. Chem. Eng. China. –2009. –Vol.3(4), –P.457.24.Pechnikova, N. L. Synthesis of meso-mono-phenylporphyrins with active groupsin the benzene rings / Pechnikova N.L., Lyubimtsev A.V., Syrbu S.A. // Russ.J. General Chem. –2013. –Vol. 83, № 1. –P. 99–105.25.Lindsey, J.S. Visible light-harvesting in covalently-linked porphyrin-cyanine dyes/ Lindsey J.S., Brown P.A., Siese D.A. // Tetrahedron. –1989.
–Vol.45, № 15. –P. 4845–4866.26.Fungo, F. Synthesis of porphyrin dyads with potential use in solar energyconversion / Fungo F., Otero L.O., Sereno L., Sillber J.J., Durantini E.D. // J.Mater.Chem. –2000. –Vol. 10. –P. 645–650.27.Lee, C.H. One-flask synthesis ofmeso-substituted dipyrromethanes and theirapplication in the synthesis oftrans-substituted porphyrin building blocks / Lee C.H., LindseyJ.S.
//Tetrahedron. –1994. –Vol. 50, № 39, –P. 11427–11440.28.Shanmugathasan, S. Advances in modern synthetic porphyrin chemistry /Shanmugathasan S., Edwards C., Boyle R.W. // Tetrahedron. –2000. –Vol.56, № 8. –P.1025–1046.29.Bhaumik, J. Synthesis and Photophysical Properties of SulfonamidophenylPorphyrinsas Models for Activatable Photosensitizers / Bhaumik J., Weissleder R., McCarthy J.R. // J. Org. Chem. –2009. –Vol. 74, –5894–5901.30.Dean, M.
L. Microwave-promoted insertion of Group 10 metals into free baseporphyrins and chlorins: scope and limitations / Dean M. L., Schmink J. R., Leadbeater N. E.,Bruckner C. // DaltonTrans. –2008. –P. 1341–1345.31.Melomedov, J. Porphyrin amino acids–amide coupling, redox andphotophysicalproperties of bis(porphyrin) amides / Melomedov J., Wünsche von Leupoldt A., MeisterM.,Laquai F., Heinze K.
// Dalton Trans. –2013. –Vol. 42. –P. 9727–9739.14332.Lindsey, J. S. Synthetic Routes to meso-Patterned Porphyrins / Lindsey J. S. //Acc. Chem. Res. –2010. –Vol. 43, №2. –P. 300–311.33.Pisarek, S. Strategies toward the synthesis of amphiphilic porphyrins / Pisarek S.,Maximova K., Gryko D. // Tetrahedron.
–2014. –Vol. 70. –P.6685–6715.34.Lindsey, J. S. Rothemund and Adler-Longo reactions revisited: synthesis oftetraphenylporphyrins under equilibrium conditions / Lindsey J. S., Schreiman I. C., Hsu H. C.,Kearney P. C., Marguerettaz A. M. // J. Org. Chem . –1987.
–Vol. 52, № 5. –P. 827–836.35.Сырбу, С.А. Синтез (гидроксифенил)порфиринов / Сырбу С.А., СемейкинА.С. // Ж.ОрХ. 1999. Т.35. В. 8.С.1262-1265.36.Сырбу С.А.Мезо-фенилзамещенныепорфирины.Модификацияв арильных группах / Сырбу С.А., Семейкин А.С., Койфман О.И. // Изв. вузов. Химия ихим. технол. –2004. –Т.47. №5. –С.46-55.37.Bonar-Law, R. P. Porphyrin Synthesis in Surfactant Solution: MulticomponentAssembly in Micelles / Bonar-Law R. P. //J. Org.
Chem. –1996. – Vol. 61. – P.3623–3634.38.Wang, T. Langmuir–Schaefer films of a set of achiral amphiphilic porphyrins:aggregation and supramolecular chirality / Wang T., Liu M. // Soft Matter. –2008. –Vol. 4. –P.775–78339.Daphnomili, D.Synthetic Approach of New Trans-SubstitutedHydroxylporphyrins/ Daphnomili D., Grammatikopoulou M., Raptopoulou C., Charalambidis G., Lazarides T.,Coutsolelos A. G.
// Bioinorganic Chemistry and Applications. 2010. Article ID 307696, 6pages. doi:10.1155/2010/30769640.Littler, B. J. Investigation of Conditions Giving Minimal Scrambling in theSynthesis of trans-Porphyrins from Dipyrromethanes and Aldehydes / Littler B. J., Ciringh Y.,Lindsey J. S. // J.
Org. Chem. –1999. –Vol. 6. –P. 2864–287241.Ogura, H. Trans-Disubstituted Tetraarylporphyrin as a Precursor to LargerMolecular Architectures: An Application of MacDonald “2 + 2” Porphyrin Synthesis in AqueousAnionic Surfactant / Ogura H., WalkerA. F. // Inorg. Chem. –2001. –Vol. 40. –P.5729–573242.Семейкин А.С., Сырбу С.А., КойфманО.И. // Изв.
вузов. Химия и хим.Технология. –2004. –Т. 47. –С. 46.43.Yu, M. Synthesis, spectroscopy, surface photovoltage, and electrochemicalproperties of porphyrin compound liquid crystals / Yu M., Liu G.F., Cui X.L. // J. PorphyrinsPhthalocyanines. 2005. –Vol. 9. – P.231.44.Герасимова, O.A.. Synthesis of 5-(4-hydroxyphenyl)-10,15,20-tris[3,5-di(tert-butyl)-4-hydroxyphenyl]porphine and 5-(4-palmitoyloxyphenyl)-10,15,20-tris[3,5-di(tert-butyl)1444-hydroxyphenyl]porphine and generation of phenoxyl radicals from them / O.A. Герасимова,E.Р.Милаева, Д.Б.Шпаковский, A.С.Семейкин, С.A.Сырбу // Russ.
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