Синтез и исследование краунсодержащих полигетероциклических производных (1105711), страница 25
Текст из файла (страница 25)
100. – № 7. – P. 2537-2574.32.Kim J., Yoon D., Lee S.H., Ko S., Lee Y-S., Zong K. An efficient synthesis ofthiophene/pyrrol-fused crown ethers using Mitsunobu reaction for potential application tosensory electroactivepolymers // Bulletin of the Korean Chemical Society. – 2006. – Vol. 27. –№ 11. – P.
1910-1912.33.Rimmel G., Bäuerle P. Molecular recognition properties of crown ether-functionalizedoligothiophenes // Synthetic Metals. – 1999. – Vol. 102. – № 1-3. – P. 1323-1324.34.Berlin A., Zotti G., Zecchin S., Schiavon G. EQCM analysis of alkali metal ioncoordination properties of novel poly(thiophene)s 3,4-functionalized with crown-ether moieties// Synthetic Metals. – 2002. – Vol. 131. – № 1-3.
– P.149-160.35.Miyazaki Y., Kanbara T., Osakada K., Yamamoto T., Kubota K. A New type ofpoly(thiophene-2,5-diyl) having a crown etheral subunit. Strong interaction of the subunit with158cationic dopants to exhibit unique doping-undoping behavior // Polymer Journal. – 1994. – Vol.26. – № 4. – P. 509-512.36.Miyazaki Y., Yamamoto T. Polythiophene derivatives having crown-etheral subunitprepared by dehalogenation polycondensation with Ni(0)-complex // Synthetic Metals. – 1995.
–Vol. 69. – № 1-3. – P. 317-318.37.Yamamoto T., Omote M., Miyazaki Y., Kashiwazaki A., Lee B., Kanbara T., OsakadaK., Inoue T., Kubota K. Poly(thiophene-2,5-diyl)s with a crown etheral subunit. Preparation,optical properties, and n-doped state stabilized against air // Macromolecules. – 1997. – Vol. 30.– № 23. – P. 7158-7165.38.Casanovas J., Zanuy D., Alemán C. Structural and electronic properties of crown etherfunctionalized oligothiophenes // Macromolecules.
– 2008. – Vol. 41. – № 11. – P. 3919-3924.39.Casanovas J., Alemán C. Comparative theoretical study of heterocyclic conductingoligomers: neutral and oxidized forms // Journal of Physycal Chemistry C. – 2007. – Vol. 111. –№ 12. – P. 4823-4830.40.Casanovas J., Preat J., Zanuy D., Alemán C. Sensing abilities of crown etherfunctionalized polythiophenes // Chemistry – A European Journal. – 2009.
– Vol. 15. – № 18. –P. 4676-4684.41.Scheib S., Bauerle P. Synthesis and characterization of oligo- and crown ether-substitutedpolythiophenes – a comparative study // Journal of Materials Chemistry. – 1999. – № 9. – P.2139-2150.42.Мизерев А.А., Луковская Е.В., Бобылева А.А., Федорова О.А., Федоров Ю.В.,Анисимов А.В. Синтез, комплексообразование, оптические и электрохимические свойстваолиготиофенов. // Успехи в химии и химической технологии. Сборник научных трудовРХТУ им. Д.И. Менделеева. – 2010. – Вып. 24. – № 5.
– C. 89-92.43.Halfpenny J., Rooney P.B., Sloman Z.S. A facile route to a novel aza-crown etherincorporating three thiophene moieties // Tetrahedron Letters. – 2000. – Vol. 41. – № 32. – P.6223-6226.44.BlanchardP.,JousselmeB.,FrèreP.,RoncaliJ.3-and3,4-Bis(2-cyanoethylsulfanyl)thiophenes as building blocks for functionalized thiophene-based πconjugated systems // Journal of Organic Chemistry. – 2002. – Vol. 67.
– № 11. – P. 3961-3964.45.Bäuerle P., Scheib S. Molecular Recognition of alkali ions by crown ether functionalizedPoly(alkylthiophenes). // Advanced Materials. – 1993. – Vol. 5. – № 11. – P. 848-853.46.Bäuerle P., Götz G., Hiller, M., Scheib S., Fischer T., Segelbacher U., Bennati M., GruppA., Mehring M., Stoldt M., Seidel C., Geiger F., Schweizer H., Umbach E., Schmelzer M., Roth159S., Egelhaaf H.J., Oelkrug D., Emele P., Port H.
Design, synthesis and assembly of newthiophene-based molecular functional units with controlled properties // Synthetic Metals. –1993. – Vol. 61. – № 1-2. – P. 71-79.47.Bradshaw J.S., Izatt R.M., Bordunov A.V., Zhu C.Y., Hathaway J.K. Comprehensivesupramolecular chemistry / Oxford: Pergamon, 1996. Vol. 1, Chapter 2.48.Boldea A., Lévesque I., Leclerc M. Controlled ionochromism with polythiophenesbearing crown ether side chains // Journal of Materials Chemistry.
– 1999. – № 9. – P. 21332138.49.Si P., Chi Q., Li Z., Ulstrup J., Moller P.J., Mortensen J. Functional polythiophenenanoparticles: size-controlled electropolymerization and ion selective response // Journal ofAmerican Chemical Society.
– 2007. – Vol. 129. – № 13. – P. 3888-3896.50.Simionescu C.I., Cianga I., Ivanoiu M., Duca Al., Cocarla I, Grigoras M. Synthesis andelectrochemical polymerization of some monomers with Schiff base or vinylene structures andthiophene moieties // European Polymer Journal. – 1999. – Vol. 35. – № 4. – P.
587-599.51.Bernier S., Garreau S., Béra-Abérem M., Gravel C., Leclerc M. A Versatile approach toaffinitychromic polythiophenes // Journal of American Chemical Society. – 2002. – Vol. 124. –№ 42. – P. 12463-12468.52.Lukovskaya E., Bobyleva A., Fedorova O., Fedorov Yu., Anisimov A., Didane Y.,Brisset H., Fages F. Novel crown-containing 3-styryl derivatives of oligothiophenes: synthesis,structure, and optical and electrochemical characteristics // Russian Chemical Bulletin.
– 2009. –Vol. 58. – № 7. – P. 1509-1515.53.Lukovskaya E., Bobylyova A., Fedorova O., Fedorov Y., Kardashev S., Maksimov A.,Anisimov A., Maurel F., Marmois E., Jonusauskas G., Didane Y., Brisset H., Fages F.Investigation of crown-containing styrylthiophene derivatives which are optically andelectrochemically sensitive to the presence of metal cations // Synthetic Metals. – 2007. – Vol.157. – № 22-23.
– P.885–893.54.Fedorova O., Lukovskaya E., Mizerev A., Fedorov Y., Bobylyova A., Maksimov A.,Moiseeva A., Anisimov A., Jonusauskas G. Synthesis and multiparameter sensor properties ofthe crown-containing thiophene derivatives // Journal of Physical Organic Chemistry. – 2010. –Vol. 23. – № 3. – P. 246-254.55.Lukovskaya E.V., Bobyleva A.A., Mizerev A.A., Fedorova O.A., Fedorov Yu.V.,Moiseeva A.A., Anisimov A.V. A multiparametric sensor for cationic analysis // Russian Journalof Physical Chemistry.
– 2010. – Vol. 84. – № 12. – P. 2088-2091.16056.Lukovskaya E., Bobylyova A., Fedorov Y., Maksimov A., Anisimov A., Fedorova O.,Jonusauskas G., Fages F. Metal ion modulated torsion angle in a ditopic oligothiophene ligand:Toward supramolecularcontrol of π-conjugation // ChemPhysChem. – 2010. – Vol. 11. – № 14. –P.3152-3160.57.Clarke T.M., Gordon K.C., Kwok W.M., Phillips D.L., Officer D.L. Tuning from π,π* tocharge-transfer excited states in styryl-substituted terthiophenes: An ultrafast and steady-stateemission study // Journal of Physical Chemistry.
– 2006. – Vol. 110. – № 24. – P. 7696-7702.58.Batista R.M.F., Oliveira E., Costa S.P., Lodeiro C., Raposo M.M.M. Synthesis andevaluation of bipendant-armed (oligo)thiophene crown ether derivatives as new chemical sensors// Tetrahedron Letters. – 2008. – Vol. 49. – № 46.
– P. 6575-6578.59.Almeida S., Rivera E., Reyna-González J.M., Huerta G., Tapia F., Aguilar-Martínez M.Synthesis and characterization of novel polythiophenes bearing oligo(ethylene glycol) spacersand crown ethers // Synthetic Metals. – 2009. – Vol. 159. – № 12. – P. 1215-1223.60.Leclerc M. Optical and electrochemical transducers based on functionalizedconjugatedpolymers // Advanced Materials. – 1999.
– Vol. 11. – № 18. – P. 1491-1498.61.Pedras B., Fernandez L., Oliveira E., Rodríguez L., Raposo M.M.M., Capelo J.L.,Lodeiro C. Synthesis, characterization and spectroscopic studies of two new Schiff-basebithienyl pendant-armed 15-crown-5 molecular probes // Inorganic Chemistry Communications.– 2009. – Vol.
12. – № 2. – P. 79-85.62.Oliveira E., Batista R.M.F., Costa S.P.G., Raposo M.M.M., Lodeiro C. Exploring theemissive properties of new azacrown compounds bearing aryl, furyl, or thienyl moieties: Aspecial case of chelation enhancement of fluorescence upon interaction with Ca2+, Cu2+, or Ni2+// Inorganic Chemistry. – 2010. – Vol. 49. – № 23. – P. 10847-10857.63.Qin W., Baruah M., Sitwa M., Van der Auweraer M., De Borggraeve W.M., Beljonne D.,Averbeke B.V., Boens N.J. Ratiometric, fluorescent BODIPY dye with aza crown etherfunctionality: synthesis, solvatochromism, and metal ion complex formation // Journal ofPhysical Chemistry A.
– 2008. – Vol. 112. – № 27. – P. 6104-6114.64.Warmke H., Wiczk W., Ossowski T. Interactions of metal ions with monoaza crownethers A15C5 and A18C6 carrying dansyl fluorophore as pendant in acetonitrile solution //Talanta. – 2000. – Vol. 52. – № 3. – P. 449-456.65.Lever A.B.P. Inorganic Electronic Spectroscopy / Amsterdam: Elsevier, 1968.66.Batista R.M.F., Oliveira E., Costa S.P.G., Lodeiro C., Raposo M.M.M.
(Oligo)thienyl-imidazo-benzocrown ether derivatives: Synthesis, photophysical studies and evaluation of theirchemosensory properties // Talanta. – 2011. – Vol. 85. – № 5. – P. 2470-2478.16167.Raposo M.M.M., Kirsch G. Formylation, dicyanovinylation and tricyanovinylation of 5-alkoxy- and 5-amino- substituted 2,2'-bithiophenes // Tetrahedron. – 2003.
– Vol. 59. – № 26. –P. 4891-4899.68.Batista R.M.F., Costa S.P.G., Belsley M., Lodeiro C., Raposo M.M.M. Synthesis andcharacterization of novel (oligo)thienyl-imidazo-phenanthrolines as versatile p-conjugatedsystems for several optical applications // Tetrahedron.
– 2008. – Vol. 64. – № 39. – P. 92309238.69.Batista R.M.F., Oliveira E., Costa S.P.G., Lodeiro C., Raposo M.M.M. Synthesis and IonSensing Properties of New Colorimetric and Fluorimetric Chemosensors Based on BithienylImidazo-Anthraquinone Chromophores // Organic Letters. – 2007. – Vol. 9. – № 17. – P. 32013204.70.Batista R.M.F., Oliveira E., Costa S.P.G., Lodeiro C., Raposo M.M.M. Imidazo-benzo-15-crown-5 ethers bearing arylthienyl and bithienyl moieties as novel fluorescent chemosensorsfor Pd2+ and Cu2+ // Tetrahedron.
– 2011. – Vol. 67. – № 37. – P. 7106-7113.71.Wu Y.X., Cao J., Deng H.Y., Feng J.X. Synthesis, complexation, and fluorescencebehavior of 3,4-dimethylthieno[2,3-b]thiophene carrying two monoaza-15-crown-5 ether groups// Spectrochimica Acta Part A. – 2011. – Vol. 82. – №1. – P. 340-344.72.Sannicolò F., Brenna E., Benincori T., Zotti G., Zecchin S., Schiavon G., Pilati T. HighlyOrdered poly(cyclopentabithiophenes) functionalized with crown-ether moieties forlithium andsodium-sensing electrodes // Chemistry of Materials. – 1998.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
