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NTIS 바로가기Journal of fluorescence, v.24 no.6, 2014년, pp.1553 - 1561
Saleem, Muhammad , Ali, Anser , Park, Bong Joo , Choi, Eun Ha , Lee, Ki Hwan
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Dyes Pigm S Li 93 1422 2012 10.1016/j.dyepig.2011.10.004 Li S, He D (2012) Synthesis and optical properties of novel anthracene-based stilbene derivatives containing an 1,3,4-oxadiazole unit. Dyes Pigm 93:1422-1427
J Phys Chem C X Xu 112 874 2008 10.1021/jp076992d Xu X, Peng B, Chen J, Liang M, Cai F (2008) New triphenylamine-based dyes for dye-sensitized solar cells. J Phys Chem C 112:874-880
Chem Asian J KR Thomas 7 738 2012 10.1002/asia.201100849 Thomas KR, Kapoor N, Lee CP, Ho KC (2012) Organic dyes containing pyrenylamine-based cascade donor systems with different aromatic π linkers for dye-sensitized solar cells: optical, electrochemical, and device characteristics. Chem Asian J 7:738-750
J Phys Chem C A Dualeh 116 1572 2012 10.1021/jp209691e Dualeh A, Angelis FD, Fantacci S, Moehl T, Yi C, Kessler F, Baranoff E, Nazeeruddin MK, Gratzel M (2012) Influence of donor groups of organic D − π-a dyes on open-circuit voltage in solid-state dye-sensitized solar cells. J Phys Chem C 116:1572-1578
Chem Mater KRJ Thomas 20 1830 2008 10.1021/cm702631r Thomas KRJ, Hsu YC, Lin JT, Lee KM, Ho KC, Lai CH, Cheng YM, Chou PT (2008) 2,3-Disubstituted thiophene-based organic dyes for solar cell. Chem Mater 20:1830-1840
J Am Chem Soc AS Galvez 122 2911 2000 10.1021/ja993985x Galvez AS, Hunt P, Robb MA, Olivucci M, Vreven T, Schlegel HB (2000) Ultrafast radiationless deactivation of organic dyes: evidence for a two-state two-mode pathway in polymethine cyanines. J Am Chem Soc 122:2911-2924
Chem Eur J DF Chen 16 12873 2010 10.1002/chem.201001294 Chen DF, Chang CW, Lin JL, Hsu YC, Yeh MCP, Hsu CP, Sun SS (2010) Photophysical studies of dipolar organic dyes that feature a 1,3-cyclohexadiene conjugated linkage: the implication of a twisted intramolecular charge-transfer state on the efficiency of dye-sensitized solar cells. Chem Eur J 16:12873-12882
Dyes Pigm MA Eid 104 197 2014 10.1016/j.dyepig.2014.01.004 Eid MA, Lim SH, Park KW, Fitzpatrick B, Han CH, Kwak K, Hong J, Cooke G (2014) Facile synthesis of metal-free organic dyes featuring a thienylethynyl spacer for dye sensitized solar cell. Dyes Pigm 104:197-203
J Phys Chem C M Pastore 114 7205 2010 10.1021/jp100713r Pastore M, Mosconi E, Angelis FD, Gratzel M (2010) A computational investigation of organic dyes for dye-sensitized solar cells: benchmark, strategies, and open issues. J Phys Chem C 114:7205-7212
Tetrahedron Lett K Ono 49 5816 2008 10.1016/j.tetlet.2008.07.122 Ono K, Ito H, Nakashima A, Uemoto M, Tomura M, Saito K (2008) Synthesis and properties of naphthalene trimers linked by 1,3,4-oxadiazole spacers. Tetrahedron Lett 49:5816-5819
J Lumin H Yang 131 749 2011 10.1016/j.jlumin.2010.11.030 Yang H, Ge YQ, Jia J, Wang JW (2011) Synthesis and optical properties of novel pyrido [1,2-a] benzimidazole-containing 1,3,4-oxadiazole derivatives. J Lumin 131:749-755
J Lumin YQ Ge 131 1070 2011 10.1016/j.jlumin.2011.01.024 Ge YQ, Hao BQ, Duan GY, Wang JW (2011) The synthesis, characterization and optical properties of novel 1,3,4-oxadiazole-containing imidazo [1,5-a] pyridine derivatives. J Lumin 131:1070-1076
Dyes Pigm HS Lv 86 25 2010 10.1016/j.dyepig.2009.11.003 Lv HS, Zhao BX, Li JK, Xia Y, Lian S, Liu WY, Gong ZL (2010) The synthesis, characterization and optical properties of novel, substituted, pyrazoly 1,3,4-oxadiazole derivatives. Dyes Pigm 86:25-31
Int J Mol Sci TY Wu 11 329 2010 10.3390/ijms11010329 Wu TY, Tsao MH, Chen FL, Su SG, Chang CW, Wang HP, Lin YC, Yang WCO, Sun IW (2010) Synthesis and characterization of organic dyes containing various donors and acceptors. Int J Mol Sci 11:329-353
Chem Cent J P Zucca 6 161 2012 10.1186/1752-153X-6-161 Zucca P, Rescigno A, Pintus M, Rinaldi AC, Sanjust E (2012) Degradation of textile dyes using immobilized lignin peroxidase-like metalloporphines under mild experimental conditions. Chem Cent J 6:161-168
Int J Environ Sci PBS Ratna 3 940 2012 Ratna PBS (2012) Pollution due to synthetic dyes toxicity & carcinogenicity studies and remediation. Int J Environ Sci 3:940-955
10.1002/ejoc.200500372 Arunkumar E. Forbes CC. Smith BD (2005) Improving the Properties of Organic Dyes by Molecular Encapsulation. Eur. J. Org. Chem. 4051-4059. DOI: 10.1002/ejoc.200500372
Phys Rev Res Int OO Ajani 3 24 2013 Ajani OO, Akinremi OE, Ajani AO, Osoh AE, Anake WU (2013) Synthesis and spectroscopic study of naphtholic and phenolic azo dyes. Phys Rev Res Int 3:24-41
Opt Mater ES Balcerzak 36 892 2014 10.1016/j.optmat.2013.12.017 Balcerzak ES, Konieczkowska J, Siwy M, Sobolewska A, Wojtowicz M, Wiacek M (2014) Comparative studies of polyimides with covalently bonded azo-dyes with their supramolecular analoges: thermo-optical and photoinduced properties. Opt Mater 36:892-902
IJRRAS JO Otutu 15 292 2013 Otutu JO (2013) Synthesis and application of azo dyes derived from 2-amino-1, 3,4-thiadiazole-2-thiol on polyester fibre. IJRRAS 15:292-296
Nanoscale Res Lett A Auger 6 328 2011 10.1186/1556-276X-6-328 Auger A, Samuel J, Poncelet O, Raccurt O (2011) A comparative study of non-covalent encapsulation methods for organic dyes into silica nanoparticles. Nanoscale Res Lett 6:328-340
J Biomed Opt I Texier 14 054005 2009 10.1117/1.3213606 Texier I, Goutayer M, Silva AD, Guyon L, Djaker N (2009) Cyanine-loaded lipid nanoparticles for improved in vivo fluorescence imaging. J Biomed Opt 14:054005. doi: 10.1117/1.3213606
J Org Chem J Huang 74 2167 2009 10.1021/jo802297x Huang J, Xu Y, Qian X (2009) A rhodamine-based Hg2+ sensor with high selectivity and sensitivity in aqueous solution: a NS2-containing receptor. J Org Chem 74:2167-2170
Dyes Pigm NI Georgiev 91 332 2011 10.1016/j.dyepig.2011.04.015 Georgiev NI, Sakr AR, Bojinov VB (2011) Design and synthesis of novel fluorescence sensing perylene diimides based on photoinduced electron transfer. Dyes Pigm 91:332-339
CW Garland 630 2009 Experiments in physical chemistry 8 Garland CW, Nibler JW, Shoemaker DP (2009) Experiments in physical chemistry, 8th edn. The McGraw-Hill Companies, Inc., New York, pp 630-632
Rev J Phys Chem JN Demas 75 991 1971 10.1021/j100678a001 Demas JN, Crosby GA (1971) Measurement of photoluminescence quantum yields. Rev J Phys Chem 75:991-1024
Nat Protoc C Wurth 8 1535 2013 10.1038/nprot.2013.087 Wurth C, Grabolle M, Pauli J, Spieles M, Genger UR (2013) Relative and absolute determination of fluorescence quantum yields of transparent samples. Nat Protoc 8:1535-1550
Pure Appl Chem AM Brouwer 83 2213 2011 10.1351/PAC-REP-10-09-31 Brouwer AM (2011) Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report). Pure Appl Chem 83:2213-2228
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