-
1
-
-
30944467113
-
A guide to choosing fluorescent proteins
-
DOI 10.1038/nmeth819, PII N819
-
Shaner, N. C., Steinbach, P. A. & Tsien, R. Y. A guide to choosing fluorescent proteins. Nat. Methods 2, 905-909 (2005). (Pubitemid 43108726)
-
(2005)
Nature Methods
, vol.2
, Issue.12
, pp. 905-909
-
-
Shaner, N.C.1
Steinbach, P.A.2
Tsien, R.Y.3
-
2
-
-
0031663369
-
The green fluorescent protein
-
DOI 10.1146/annurev.biochem.67.1.509
-
Tsien, R. Y. The green fluorescent protein. Annu. Rev. Biochem. 67, 509-544 (1998). (Pubitemid 28411137)
-
(1998)
Annual Review of Biochemistry
, vol.67
, pp. 509-544
-
-
Tsien, R.Y.1
-
3
-
-
0037418882
-
Development and use of fluorescent protein markers in living cells
-
Lippincott-Schwartz, J. & Patterson, G. H. Development and use of fluorescent protein markers in living cells. Science 300, 87-91 (2003).
-
(2003)
Science
, vol.300
, pp. 87-91
-
-
Lippincott-Schwartz, J.1
Patterson, G.H.2
-
4
-
-
0036902813
-
Creating new fluorescent probes for cell biology
-
DOI 10.1038/nrm976
-
Zhang, J., Campbell, R. E., Ting, A. Y. & Tsien, R. Y. Creating new fluorescent probes for cell biology. Nat. Rev. Mol. Cell Biol. 3, 906-918 (2002). (Pubitemid 35477369)
-
(2002)
Nature Reviews Molecular Cell Biology
, vol.3
, Issue.12
, pp. 906-918
-
-
Zhang, J.1
Campbell, R.E.2
Ting, A.Y.3
Tsien, R.Y.4
-
5
-
-
84863229486
-
Colour tuning from green to red by substituent effects in phosphorescent tris-cyclometalated iridium(III) complexes of carbazole-based ligands: Synthetic, photophysical, computational and high efficiency OLED studies
-
Tavasli, M. et al. Colour tuning from green to red by substituent effects in phosphorescent tris-cyclometalated iridium(III) complexes of carbazole-based ligands: synthetic, photophysical, computational and high efficiency OLED studies. J. Mater. Chem. 22, 6419-6428 (2012).
-
(2012)
J. Mater. Chem
, vol.22
, pp. 6419-6428
-
-
Tavasli, M.1
-
6
-
-
84860380737
-
Tuning of spacer groups in organic dyes for efficient inhibition of charge recombination in dye-sensitized solar cells
-
Kim, M. J. et al. Tuning of spacer groups in organic dyes for efficient inhibition of charge recombination in dye-sensitized solar cells. Dyes Pigm. 95, 134-141 (2012).
-
(2012)
Dyes Pigm
, vol.95
, pp. 134-141
-
-
Kim, M.J.1
-
7
-
-
77957720245
-
Fluorescent chemosensor for detection and quantitation of carbon dioxide gas
-
Liu, Y. et al. Fluorescent Chemosensor for Detection and Quantitation of Carbon Dioxide Gas. J. Am. Chem. Soc. 132, 13951-13953 (2010).
-
(2010)
J. Am. Chem. Soc
, vol.132
, pp. 13951-13953
-
-
Liu, Y.1
-
8
-
-
79851502455
-
Specific detection of d-glucose by a tetraphenylethene-based fluorescent sensor
-
Liu, Y. et al. Specific Detection of D-Glucose by a Tetraphenylethene- Based Fluorescent Sensor. J. Am. Chem. Soc. 133, 660-663 (2011).
-
(2011)
J. Am. Chem. Soc
, vol.133
, pp. 660-663
-
-
Liu, Y.1
-
9
-
-
84855887357
-
Improving the contrast ratio of OLED displays: An analysis of various techniques
-
Singh, R., Unni, K. N. N., Solanki, A. & Deepak. Improving the contrast ratio of OLED displays: An analysis of various techniques. Opt. Mat. 34, 716-723 (2012).
-
(2012)
Opt. Mat
, vol.34
, pp. 716-723
-
-
Singh, R.1
Unni, K.N.N.2
Solanki, A.3
Deepak4
-
10
-
-
84862935789
-
Characterization, and OFET and OLED properties of pi-extended ladder-type heteroacenes based on indolodibenzothiophene
-
Wang, C. S., Nishida, J., Bryce, M. R. & Yamashita, Y. Synthesis, Characterization, and OFET and OLED Properties of pi-Extended Ladder-Type Heteroacenes Based on Indolodibenzothiophene. Bull. Chem. Soc. Jpn. 85, 136-143 (2012).
-
(2012)
Bull. Chem. Soc. Jpn
, vol.85
, pp. 136-143
-
-
Wang, C.S.1
Nishida, J.2
Bryce, M.R.3
Synthesis, Y.Y.4
-
11
-
-
0006483573
-
2 films
-
Oregan, B. & Gratzel, M. A Low-Cost, High-Efficiency Solar-Cell Based on Dye-Sensitized Colloidal Tio2 Films. Nature 353, 737-740 (1991). (Pubitemid 21912607)
-
(1991)
Nature
, vol.353
, Issue.6346
, pp. 737-740
-
-
O'Regan, B.1
Gratzel, M.2
-
12
-
-
80555157669
-
Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency
-
Yella, A. et al. Porphyrin-Sensitized Solar Cells with Cobalt (II/III)-Based Redox Electrolyte Exceed 12 Percent Efficiency. Science 334, 629-634 (2011).
-
(2011)
Science
, vol.334
, pp. 629-634
-
-
Yella, A.1
-
13
-
-
84864717144
-
Fluorescence and phosphorescence from higher excited states oforganic molecules
-
Itoh, T. Fluorescence and Phosphorescence from Higher Excited States ofOrganic Molecules. Chem. Rev. 112, 4541-4568 (2012).
-
(2012)
Chem. Rev
, vol.112
, pp. 4541-4568
-
-
Itoh, T.1
-
15
-
-
79959249733
-
Photoluminescent hyperbranched poly(amido amine) containing beta-cyclodextrin as a nonviral gene delivery vector
-
Chen, Y. et al. Photoluminescent Hyperbranched Poly(amido amine) Containing beta-Cyclodextrin as a Nonviral Gene Delivery Vector. Bioconjugate Chem. 22, 1162-1170 (2011).
-
(2011)
Bioconjugate Chem
, vol.22
, pp. 1162-1170
-
-
Chen, Y.1
-
16
-
-
58349088080
-
Fluorescence Investigations of Oxygen-doped Simple Amine Compared with Fluorescent PAMAM Dendrimer
-
Chu, C. C. & Imae, T. Fluorescence Investigations of Oxygen-Doped Simple Amine Compared with Fluorescent PAMAM Dendrimer. Macromol. Rapid Commun. 30, 89-93 (2009).
-
(2009)
Macromol. Rapid Commun
, vol.30
, pp. 89-93
-
-
Chu, C.C.1
Imae, T.2
-
17
-
-
77953448027
-
Fractal growth ofpamamdendrimer aggregates and its impact on the intrinsic emission properties
-
Jasmine, M. J.Prasad, E. Fractal Growth ofPAMAMDendrimer Aggregates and Its Impact on the Intrinsic Emission Properties. J. Phys. Chem. B 114, 7735-7742 (2010).
-
(2010)
J. Phys. Chem. B
, vol.114
, pp. 7735-7742
-
-
Jasmine . M, J.1
Prasad, E.2
-
18
-
-
78649421221
-
Facile one-pot approach for preparing fluorescent and biodegradable hyperbranched poly(amidoamine)s
-
Jiang, G. H., Wang, Y., Sun, X. K. & Shen, J. J. Facile one-pot approach for preparing fluorescent and biodegradable hyperbranched poly(amidoamine)s. Polym. Chem. 1, 618-620 (2010).
-
(2010)
Polym. Chem
, vol.1
, pp. 618-620
-
-
Jiang, G.H.1
Wang, Y.2
Sun, X.K.3
Shen, J.J.4
-
19
-
-
3142707418
-
Strong blue photoluminescence and ECL from OH-terminated PAMAM dendrimers in the absence of gold nanoparticles
-
DOI 10.1021/ja0475914
-
Lee, W. I., Bae, Y. J. & Bard, A. J. Strong blue photoluminescence and ECL from OH-terminated PAMAM dendrimers in the absence of gold nanoparticles. J. Am. Chem. Soc. 126, 8358-8359 (2004). (Pubitemid 38917942)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.27
, pp. 8358-8359
-
-
Lee, W.I.1
Bae, Y.2
Bard, A.J.3
-
20
-
-
79958797642
-
Unraveling the photoluminescence puzzle of PAMAM dendrimers
-
Lin, S. Y. et al. Unraveling the Photoluminescence Puzzle of PAMAM Dendrimers. Chem. Eur. J. 17, 7158-7161 (2011).
-
(2011)
Chem. Eur. J
, vol.17
, pp. 7158-7161
-
-
Lin, S.Y.1
-
21
-
-
84856289967
-
Intrinsically fluorescent PAMAM dendrimer as gene carrier and nanoprobe for nucleic acids delivery: Bioimaging and transfection study
-
Tsai, Y. J., Hu, C. C., Chu, C. C. & Toyoko, I. Intrinsically Fluorescent PAMAM Dendrimer as Gene Carrier and Nanoprobe for Nucleic Acids Delivery: Bioimaging and Transfection Study. Biomacromolecules 12, 4283-4290 (2011).
-
(2011)
Biomacromolecules
, vol.12
, pp. 4283-4290
-
-
Tsai, Y.J.1
Hu, C.C.2
Chu, C.C.3
Toyoko, I.4
-
22
-
-
33845660896
-
Fluorescence emission from PAMAM and PPI dendrimers
-
DOI 10.1016/j.jcis.2006.10.025, PII S0021979706009337
-
Wang, D., Imae, T. & Miki, M. Fluorescence emission from PAMAM and PPI dendrimers. J. Colloid Interface Sci. 306, 222-227 (2007). (Pubitemid 44960299)
-
(2007)
Journal of Colloid and Interface Science
, vol.306
, Issue.2
, pp. 222-227
-
-
Wang, D.1
Imae, T.2
Miki, M.3
-
23
-
-
73949086468
-
Synthesis and fluorescent properties of biodegradable hyperbranched Poly(amido amine)s
-
Yang, W. & Pan, C. Y. Synthesis and Fluorescent Properties of Biodegradable Hyperbranched Poly(amido amine)s. Macromol. Rapid Commun. 30, 2096-2101 (2009).
-
(2009)
Macromol. Rapid Commun
, vol.30
, pp. 2096-2101
-
-
Yang, W.1
Pan, C.Y.2
-
24
-
-
77955139276
-
Fluorescent mannose-functionalized hyperbranched poly(amido amine)s: Synthesis and interaction with E. Coli
-
Yang, W., Pan, C. Y., Luo, M. D. & Zhang, H. B. Fluorescent Mannose-Functionalized Hyperbranched Poly(amido amine)s: Synthesis and Interaction with E. coli. Biomacromolecules 11, 1840-1846 (2010).
-
(2010)
Biomacromolecules
, vol.11
, pp. 1840-1846
-
-
Yang, W.1
Pan, C.Y.2
Luo, M.D.3
Zhang, H.B.4
-
25
-
-
79955810869
-
Multiple functional hyperbranched poly(amido amine) nanoparticles: Synthesis and application in cell imaging
-
Yang, W., Pan, C. Y., Liu, X. Q. & Wang, J. Multiple Functional Hyperbranched Poly(amido amine) Nanoparticles: Synthesis and Application in Cell Imaging. Biomacromolecules 12, 1523-1531 (2011).
-
(2011)
Biomacromolecules
, vol.12
, pp. 1523-1531
-
-
Yang, W.1
Pan, C.Y.2
Liu, X.Q.3
Wang, J.4
-
26
-
-
79955015649
-
Degradable dual ph-and temperature-responsive photoluminescent dendrimers
-
Shen, Y. Q. et al. Degradable Dual pH-and Temperature-Responsive Photoluminescent Dendrimers. Chem. Eur. J. 17, 5319-5326 (2011).
-
(2011)
Chem. Eur. J
, vol.17
, pp. 5319-5326
-
-
Shen, Y.Q.1
-
27
-
-
28944452688
-
Blue photoluminescence from hyperbranched poly(amino ester)s
-
DOI 10.1021/ma051407x
-
Wu, D. C., Liu, Y., He, C. B. & Goh, S. H. Blue photoluminescence from hyperbranched poly(amino ester)s. Macromolecules 38, 9906-9909 (2005). (Pubitemid 41785122)
-
(2005)
Macromolecules
, vol.38
, Issue.24
, pp. 9906-9909
-
-
Wu, D.1
Liu, Y.2
He, C.3
Goh, S.H.4
-
28
-
-
34547893765
-
Unprecedented blue intrinsic photoluminescence from hyperbranched and linear polyethylenimines: Polymer architectures and pH-effects
-
DOI 10.1002/marc.200700190
-
Pastor-Perez, L., Chen, Y., Shen, Z., Lahoz, A. & Stiriba, S. E. Unprecedented blue intrinsic photoluminescence from hyperbranched and linear polyethylenimines: Polymer architectures and pH-effects. Macromol. Rapid Commun. 28, 1404-1409 (2007). (Pubitemid 47252012)
-
(2007)
Macromolecular Rapid Communications
, vol.28
, Issue.13
, pp. 1404-1409
-
-
Pastor-Perez, L.1
Chen, Y.2
Shen, Z.3
Lahoz, A.4
Stiriba, S.-E.5
-
30
-
-
84862093105
-
Biocompatible polyurea dendrimers with ph-dependent fluorescence
-
Restani, R. B. et al. Biocompatible Polyurea Dendrimers with pH-Dependent Fluorescence. Angew. Chem. Int. Ed. 51, 5162-5165 (2012).
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 5162-5165
-
-
Restani, R.B.1
-
31
-
-
6044260121
-
Fluorescence emission from dendrimers and its pH dependence
-
DOI 10.1021/ja0454992
-
Wang, D. J. & Imae, T. Fluorescence emission from dendrimers and its pH dependence. J. Am. Chem. Soc. 126, 13204-13205 (2004). (Pubitemid 39382730)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.41
, pp. 13204-13205
-
-
Wang, D.1
Imae, T.2
-
32
-
-
84862093105
-
Biocompatible polyurea dendrimers with ph-dependent fluorescence
-
Restani, R. B. et al. Biocompatible Polyurea Dendrimers with pH-Dependent Fluorescence. Angew. Chem. Int. Ed 51, 5162-5165 (2012).
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 5162-5165
-
-
Restani, R.B.1
-
33
-
-
84865440874
-
CO2-induced Degradation of Amine-containing Adsorbents: Reaction Products and Pathways
-
Sayari, A., Heydari-Gorji, A. & Yang, Y. CO2-Induced Degradation of Amine-Containing Adsorbents: Reaction Products and Pathways. J. Am. Chem. Soc. 134, 13834-13842 (2012).
-
(2012)
J. Am. Chem. Soc
, vol.134
, pp. 13834-13842
-
-
Sayari, A.1
Heydari-Gorji, A.2
Yang, Y.3
-
34
-
-
0036308870
-
Reversible covalent chemistry of CO2
-
Hampe, E. M. & Rudkevich, D. M. Reversible covalent chemistry of CO2. Chem. Commun. 1450-1451 (2002).
-
(2002)
Chem. Commun
, pp. 1450-1451
-
-
Hampe, E.M.1
Rudkevich, D.M.2
-
35
-
-
0242352602
-
2 and amines
-
DOI 10.1016/j.tet.2003.09.096
-
Hampe, E. M. & Rudkevich, D. M. Exploring reversible reactions between CO2 and amines. Tetrahedron 59, 9619-9625 (2003). (Pubitemid 37357117)
-
(2003)
Tetrahedron
, vol.59
, Issue.48
, pp. 9619-9625
-
-
Hampe, E.M.1
Rudkevich, D.M.2
-
36
-
-
0242385774
-
Converting carbon dioxide into carbamato derivatives
-
Dell'Amico, D. B., Calderazzo, F., Labella, L., Marchetti, F. & Pampaloni, G. Converting carbon dioxide into carbamato derivatives. Chem. Rev. 103, 3857-3897 (2003).
-
(2003)
Chem. Rev
, vol.103
, pp. 3857-3897
-
-
Dell'Amico, D.B.1
Calderazzo, F.2
Labella, L.3
Marchetti, F.4
Pampaloni, G.5
-
37
-
-
3643089036
-
Kinetics of carbamate formation and breakdown
-
Caplow,M. Kinetics of Carbamate Formation and Breakdown. J. Am. Chem. Soc. 90, 6795-6803 (1968).
-
(1968)
J. Am. Chem. Soc
, vol.90
, pp. 6795-6803
-
-
Caplow, M.1
-
38
-
-
37049072823
-
Kinetics of the formation of n,ndialkylcarbamate from diethanolamine and carbon-dioxide in anhydrous
-
Crooks, J. E. & Donnellan, J. P. Kinetics of the Formation of N,NDialkylcarbamate from Diethanolamine and Carbon-Dioxide in Anhydrous Ethanol. J. Chem. Soc., Perkin Trans. 2 191-194 (1988).
-
(1988)
Ethanol. J. Chem. Soc. Perkin Trans
, vol.2
, pp. 191-194
-
-
Crooks, J.E.1
Donnellan, J.P.2
-
39
-
-
37049081595
-
Kinetics and Mechanism of the reaction between carbon-dioxide and amines in aqueous-solution
-
Crooks, J. E. & Donnellan, J. P. Kinetics andMechanism of the Reaction Between Carbon-Dioxide and Amines in Aqueous-Solution. J. Chem. Soc., Perkin Trans. 2 331-333 (1989).
-
(1989)
J. Chem. Soc. Perkin Trans
, vol.2
, pp. 331-333
-
-
Crooks, J.E.1
Donnellan, J.P.2
-
40
-
-
79960865959
-
CO2 absorption characteristics in aqueous k2co3/piperazine solution bynmrspectroscopy
-
Kim, Y. E., Choi, J. H.,Nam, S. C. & Yoon, Y. I. CO2 Absorption Characteristics in Aqueous K2CO3/Piperazine Solution byNMRSpectroscopy. Ind. Eng. Chem. Res. 50, 9306-9313 (2011).
-
(2011)
Ind. Eng. Chem. Res
, vol.50
, pp. 9306-9313
-
-
Kim, Y.E.1
Choi, H.2
Nam J, S.C.3
Yoon, Y.I.4
-
41
-
-
4544234205
-
Effects of chemistries of trifunctional amines on mechanisms of Michael addition polymerizations with diacrylates
-
Wu, D. C., Liu, Y., He, C. B., Chung, T. S. & Goh, S. T. Effects of chemistries of trifunctional amines on mechanisms of Michael addition polymerizations with diacrylates. Macromolecules 37, 6763-6770 (2004).
-
(2004)
Macromolecules
, vol.37
, pp. 6763-6770
-
-
Wu, D.C.1
Liu, Y.2
He, C.B.3
Chung, T.S.4
Goh, S.T.5
-
43
-
-
0014420934
-
Protonated Alkyl carbamates and their cleavage to protonated carbamic acids and alkylcarbonium ions
-
Protonated Alkyl Carbamates and Their Cleavage to Protonated Carbamic Acids and Alkylcarbonium Ions. J. Am. Chem. Soc. 90, 401-& (1968).
-
(1968)
J. Am. Chem. Soc
, vol.90
, pp. 401
-
-
-
45
-
-
0014431670
-
Carbonates and hydrogen carbonates and their cleavage to protonated carbonic acid and carbonium ions possible role of protonated carbonic acid in biological carboxylation processes
-
Protonated Carbonic Acid (Trihydroxycarbonium Ion) Protonated Alkyl (Aryl)
-
Protonated Carbonic Acid (Trihydroxycarbonium Ion) and Protonated Alkyl (Aryl) Carbonates and Hydrogen Carbonates and Their Cleavage to Protonated Carbonic Acid and Carbonium Ions Possible Role of Protonated Carbonic Acid in Biological Carboxylation Processes. J. Am. Chem. Soc. 90, 1884-& (1968).
-
(1968)
J. Am. Chem. Soc
, vol.90
, pp. 1884
-
-
-
46
-
-
33947475965
-
Proton magnetic resonance study of hindered internal rotation in som substituted n,n-dimethylamides
-
Rogers, M. T. Woodbrey, J. C. Proton Magnetic Resonance Study of Hindered Internal Rotation in Som Substituted N,N-Dimethylamides. J. Phys. Chem. 66, 540-& (1962).
-
(1962)
J. Phys. Chem
, vol.66
, pp. 540
-
-
Rogers, M.T.1
Woodbrey, J.C.2
-
47
-
-
0016856653
-
Proton Nuclear Magnetic-Resonance Study of Hindered Internal-Rotation of Dimethylamino Group of N6,N6-Dimethyladenine Hydrochloride in Aqueous-Solution
-
Pitner, T. P., Sternglanz, H., Bugg, C. E. & Glickson, J. D. Proton Nuclear Magnetic-Resonance Study of Hindered Internal-Rotation of Dimethylamino Group of N6,N6-Dimethyladenine Hydrochloride in Aqueous-Solution. J. Am. Chem. Soc. 97, 885-888 (1975).
-
(1975)
J. Am. Chem. Soc
, vol.97
, pp. 885-888
-
-
Pitner, T.P.1
Sternglanz, H.2
Bugg, C.E.3
Glickson, J.D.4
-
48
-
-
33947334491
-
Hindered rotation in N,ndimethylcarbamates
-
Lustig, E., Benson, W. R. & Duy, N. Hindered Rotation in N,NDimethylcarbamates. J. Org. Chem. 32, 851-& (1967).
-
(1967)
J. Org. Chem
, vol.32
, pp. 851
-
-
Lustig, E.1
Benson, W.R.2
Duy, N.3
-
49
-
-
0011222242
-
N-Nitroamides and N-Nitrocarbamates 3. Rotational isomerism steric effects and physical properties at low temperatures
-
White, E. H., Chen,M. C. & Dolak, L. A. N-Nitroamides and N-Nitrocarbamates. 3. Rotational Isomerism Steric Effects and Physical Properties at Low Temperatures. J. Org. Chem. 31, 3038-& (1966).
-
(1966)
J. Org. Chem
, vol.31
, pp. 3038
-
-
White, E.H.1
Chenm, C.2
Dolak, L.A.3
-
52
-
-
60849114779
-
Optical absorption and emission properties of rubrene: Insight from a combined experimental and theoretical study
-
Petrenko, T., Krylova, O., Neese, F. & Sokolowski, M. Optical absorption and emission properties of rubrene: insight from a combined experimental and theoretical study. New J. Phys. 11 (2009).
-
(2009)
New J. Phys
, vol.11
-
-
Petrenko, T.1
Krylova, O.2
Neese, F.3
Sokolowski, M.4
|