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Visible-light-induced electron transport from small to large nanoparticles in bimodal gold nanoparticle-loaded titanium(IV) oxide.

Angewandte Chemie (International ed. in English)

Naya S, Niwa T, Kume T, Tada H.
PMID: 24863051
Angew Chem Int Ed Engl. 2014 Jul 07;53(28):7305-9. doi: 10.1002/anie.201402939. Epub 2014 May 26.

A key to realizing the sustainable society is to develop highly active photocatalysts for selective organic synthesis effectively using sunlight as the energy source. Recently, metal-oxide-supported gold nanoparticles (NPs) have emerged as a new type of visible-light photocatalysts driven...

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Naya S, Niwa T, Kume T, et al. Visible-light-induced electron transport from small to large nanoparticles in bimodal gold nanoparticle-loaded titanium(IV) oxide. Angew Chem Int Ed Engl. 2014;53(28):7305-9doi: 10.1002/anie.201402939.
Naya, S., Niwa, T., Kume, T., & Tada, H. (2014). Visible-light-induced electron transport from small to large nanoparticles in bimodal gold nanoparticle-loaded titanium(IV) oxide. Angewandte Chemie (International ed. in English), 53(28), 7305-9. https://doi.org/10.1002/anie.201402939
Naya, Shin-Ichi, et al. "Visible-light-induced electron transport from small to large nanoparticles in bimodal gold nanoparticle-loaded titanium(IV) oxide." Angewandte Chemie (International ed. in English) vol. 53,28 (2014): 7305-9. doi: https://doi.org/10.1002/anie.201402939
Naya S, Niwa T, Kume T, Tada H. Visible-light-induced electron transport from small to large nanoparticles in bimodal gold nanoparticle-loaded titanium(IV) oxide. Angew Chem Int Ed Engl. 2014 Jul 07;53(28):7305-9. doi: 10.1002/anie.201402939. Epub 2014 May 26. PMID: 24863051.
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Bulk size crystal growth, spectroscopic, dielectric and surface studies of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS): A potential THz crystal of stilbazolium family.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Antony Raj A, John Sundaram S, Gunaseelan R, Sagayaraj P.
PMID: 26010563
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Oct 05;149:957-64. doi: 10.1016/j.saa.2015.05.022. Epub 2015 May 11.

The synthesis and growth of a potentially useful and efficient nonlinear optical organic single crystal of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS) is reported. The growth experiment involved the slope nucleation method coupled with slow cooling as well as slow solvent evaporation...

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Antony Raj A, John Sundaram S, Gunaseelan R, et al. Bulk size crystal growth, spectroscopic, dielectric and surface studies of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS): A potential THz crystal of stilbazolium family. Spectrochim Acta A Mol Biomol Spectrosc. 2015;149:957-64doi: 10.1016/j.saa.2015.05.022.
Antony Raj, A., John Sundaram, S., Gunaseelan, R., & Sagayaraj, P. (2015). Bulk size crystal growth, spectroscopic, dielectric and surface studies of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS): A potential THz crystal of stilbazolium family. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 149957-64. https://doi.org/10.1016/j.saa.2015.05.022
Antony Raj, A, et al. "Bulk size crystal growth, spectroscopic, dielectric and surface studies of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS): A potential THz crystal of stilbazolium family." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 149 (2015): 957-64. doi: https://doi.org/10.1016/j.saa.2015.05.022
Antony Raj A, John Sundaram S, Gunaseelan R, Sagayaraj P. Bulk size crystal growth, spectroscopic, dielectric and surface studies of 4-N,N-dimethylamino-4-N'-methylstilbazolium m-nitrobenzenesulfonate (DSMNS): A potential THz crystal of stilbazolium family. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Oct 05;149:957-64. doi: 10.1016/j.saa.2015.05.022. Epub 2015 May 11. PMID: 26010563.
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Correlations between theoretical and experimental determination of heat of formation of certain aromatic nitro compounds.

Computers & chemistry

Chen C, Wu JC.
PMID: 11219427
Comput Chem. 2001 Mar;25(2):117-24. doi: 10.1016/s0097-8485(00)00073-5.

Heats of formation of energetic materials can be obtained either experimentally or theoretically. In order to compare the results of the two methods, some correlation methods were proposed in this study. The molecular structures and heats of formation of...

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Chen C, Wu JC. Correlations between theoretical and experimental determination of heat of formation of certain aromatic nitro compounds. Comput Chem. 2001;25(2):117-24doi: 10.1016/s0097-8485(00)00073-5.
Chen, C., & Wu, J. C. (2001). Correlations between theoretical and experimental determination of heat of formation of certain aromatic nitro compounds. Computers & chemistry, 25(2), 117-24. https://doi.org/10.1016/s0097-8485(00)00073-5
Chen, C, and Wu, J C. "Correlations between theoretical and experimental determination of heat of formation of certain aromatic nitro compounds." Computers & chemistry vol. 25,2 (2001): 117-24. doi: https://doi.org/10.1016/s0097-8485(00)00073-5
Chen C, Wu JC. Correlations between theoretical and experimental determination of heat of formation of certain aromatic nitro compounds. Comput Chem. 2001 Mar;25(2):117-24. doi: 10.1016/s0097-8485(00)00073-5. PMID: 11219427.
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Copper-Catalyzed Direct Amination of Nitrobenzenes with O-Alkylhydroxylamines.

The Journal of organic chemistry

Seko S, Kawamura N.
PMID: 11666957
J Org Chem. 1996 Jan 26;61(2):442-443. doi: 10.1021/jo951903r.

No abstract available.

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Seko S, Kawamura N. Copper-Catalyzed Direct Amination of Nitrobenzenes with O-Alkylhydroxylamines. J Org Chem. 1996;61(2):442-443doi: 10.1021/jo951903r.
Seko, S., & Kawamura, N. (1996). Copper-Catalyzed Direct Amination of Nitrobenzenes with O-Alkylhydroxylamines. The Journal of organic chemistry, 61(2), 442-443. https://doi.org/10.1021/jo951903r
Seko, Shinzo, and Kawamura, Norio. "Copper-Catalyzed Direct Amination of Nitrobenzenes with O-Alkylhydroxylamines." The Journal of organic chemistry vol. 61,2 (1996): 442-443. doi: https://doi.org/10.1021/jo951903r
Seko S, Kawamura N. Copper-Catalyzed Direct Amination of Nitrobenzenes with O-Alkylhydroxylamines. J Org Chem. 1996 Jan 26;61(2):442-443. doi: 10.1021/jo951903r. PMID: 11666957.
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Nitrolysis of a Highly Deactivated Amide by Protonitronium. Synthesis and Structure of HNFX(1).

The Journal of organic chemistry

Chapman RD, Gilardi RD, Welker MF, Kreutzberger CB.
PMID: 11674169
J Org Chem. 1999 Feb 05;64(3):960-965. doi: 10.1021/jo9819640.

Efficient N-nitrolysis of highly deactivated 3,3,7,7-tetrakis(difluoramino)octahydro-1,5-bis(4-nitrobenzenesulfonyl)-1,5-diazocine (1) has been achieved by the use of protonitronium reagent formed in the system nitric acid-trifluoromethanesulfonic acid, producing 3,3,7,7-tetrakis(difluoramino)octahydro-1,5-dinitro-1,5-diazocine (HNFX, 2) in 65% yield in a nonoptimized reaction. The crystal structure of the...

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Chapman RD, Gilardi RD, Welker MF, et al. Nitrolysis of a Highly Deactivated Amide by Protonitronium. Synthesis and Structure of HNFX(1). J Org Chem. 1999;64(3):960-965doi: 10.1021/jo9819640.
Chapman, R. D., Gilardi, R. D., Welker, M. F., & Kreutzberger, C. B. (1999). Nitrolysis of a Highly Deactivated Amide by Protonitronium. Synthesis and Structure of HNFX(1). The Journal of organic chemistry, 64(3), 960-965. https://doi.org/10.1021/jo9819640
Chapman, Robert D., et al. "Nitrolysis of a Highly Deactivated Amide by Protonitronium. Synthesis and Structure of HNFX(1)." The Journal of organic chemistry vol. 64,3 (1999): 960-965. doi: https://doi.org/10.1021/jo9819640
Chapman RD, Gilardi RD, Welker MF, Kreutzberger CB. Nitrolysis of a Highly Deactivated Amide by Protonitronium. Synthesis and Structure of HNFX(1). J Org Chem. 1999 Feb 05;64(3):960-965. doi: 10.1021/jo9819640. PMID: 11674169.
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Kinetic Studies of the Alkylation of Metal Cyanide Complexes: M(CO)(x)()(L)(5)(-)(x)()CN (M = Mn, Re) and CpM'(CO)(x)()(L)(2)(-)(x)()CN (M' = Fe, Ru).

Inorganic chemistry

Cardoza LA, Angelici RJ.
PMID: 11670937
Inorg Chem. 1999 Apr 19;38(8):1708-1712. doi: 10.1021/ic981014x.

Reaction rates for the alkylation of Mn(CO)(dppm)(2)CN (dppm = PPh(2)CH(2)PPh(2)), Mn(CO)(2)(tripod)CN [tripod = (PPh(2)CH(2))(3)CCH(3)], Re(CO)(3)(dppm)CN, (eta(6)-C(6)Me(6))Mn(CO)(2)CN, CpFe(dppe)CN (dppe = PPh(2)CH(2)CH(2)PPh(2)), CpRu(dppe)CN, and CpRu(CO)(PPh(3))CN with methyl 4-nitrobenzenesulfonate (MeONs) to produce complexes of the type [L(n)()M-CNMe](+) (-)ONs were investigated in 1,2-dichloroethane...

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Cardoza LA, Angelici RJ. Kinetic Studies of the Alkylation of Metal Cyanide Complexes: M(CO)(x)()(L)(5)(-)(x)()CN (M = Mn, Re) and CpM'(CO)(x)()(L)(2)(-)(x)()CN (M' = Fe, Ru). Inorg Chem. 1999;38(8):1708-1712doi: 10.1021/ic981014x.
Cardoza, L. A., & Angelici, R. J. (1999). Kinetic Studies of the Alkylation of Metal Cyanide Complexes: M(CO)(x)()(L)(5)(-)(x)()CN (M = Mn, Re) and CpM'(CO)(x)()(L)(2)(-)(x)()CN (M' = Fe, Ru). Inorganic chemistry, 38(8), 1708-1712. https://doi.org/10.1021/ic981014x
Cardoza, Laurie A., and Angelici, Robert J.. "Kinetic Studies of the Alkylation of Metal Cyanide Complexes: M(CO)(x)()(L)(5)(-)(x)()CN (M = Mn, Re) and CpM'(CO)(x)()(L)(2)(-)(x)()CN (M' = Fe, Ru)." Inorganic chemistry vol. 38,8 (1999): 1708-1712. doi: https://doi.org/10.1021/ic981014x
Cardoza LA, Angelici RJ. Kinetic Studies of the Alkylation of Metal Cyanide Complexes: M(CO)(x)()(L)(5)(-)(x)()CN (M = Mn, Re) and CpM'(CO)(x)()(L)(2)(-)(x)()CN (M' = Fe, Ru). Inorg Chem. 1999 Apr 19;38(8):1708-1712. doi: 10.1021/ic981014x. PMID: 11670937.
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Epoxide formation by ring closure of the cinnamyloxy radical.

Organic letters

Amaudrut J, Wiest O.
PMID: 10810720
Org Lett. 2000 May 04;2(9):1251-4. doi: 10.1021/ol005749t.

[formula: see text] The cinnamyloxy and oxiranyl benzyl radicals were generated by photolysis of alkyl 4-nitrobenzenesulfenates. The yet unprecedented epoxide ring formation from a primary alkoxy radical was observed. Experimental evidence supports the fact that the mode of ring...

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Amaudrut J, Wiest O. Epoxide formation by ring closure of the cinnamyloxy radical. Org Lett. 2000;2(9):1251-4doi: 10.1021/ol005749t.
Amaudrut, J., & Wiest, O. (2000). Epoxide formation by ring closure of the cinnamyloxy radical. Organic letters, 2(9), 1251-4. https://doi.org/10.1021/ol005749t
Amaudrut, and Wiest. "Epoxide formation by ring closure of the cinnamyloxy radical." Organic letters vol. 2,9 (2000): 1251-4. doi: https://doi.org/10.1021/ol005749t
Amaudrut J, Wiest O. Epoxide formation by ring closure of the cinnamyloxy radical. Org Lett. 2000 May 04;2(9):1251-4. doi: 10.1021/ol005749t. PMID: 10810720.
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Structures of three substituted arenesulfonamides from X-ray powder diffraction data using the differential evolution technique.

Acta crystallographica. Section B, Structural science

Tremayne M, Seaton CC, Glidewell C.
PMID: 12324695
Acta Crystallogr B. 2002 Oct;58:823-34. doi: 10.1107/s0108768102011928. Epub 2002 Sep 24.

The structures of three substituted arenesulfonamides have been solved from laboratory X-ray powder diffraction data, using a new direct-space structure solution method based on a differential evolution algorithm, and refined by the Rietveld method. In 2-toluenesulfonamide, C(7)H(9)NO(2)S (I) (tetragonal...

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Tremayne M, Seaton CC, Glidewell C. Structures of three substituted arenesulfonamides from X-ray powder diffraction data using the differential evolution technique. Acta Crystallogr B. 2002;58:823-34doi: 10.1107/s0108768102011928.
Tremayne, M., Seaton, C. C., & Glidewell, C. (2002). Structures of three substituted arenesulfonamides from X-ray powder diffraction data using the differential evolution technique. Acta crystallographica. Section B, Structural science, 58823-34. https://doi.org/10.1107/s0108768102011928
Tremayne, Maryjane, et al. "Structures of three substituted arenesulfonamides from X-ray powder diffraction data using the differential evolution technique." Acta crystallographica. Section B, Structural science vol. 58 (2002): 823-34. doi: https://doi.org/10.1107/s0108768102011928
Tremayne M, Seaton CC, Glidewell C. Structures of three substituted arenesulfonamides from X-ray powder diffraction data using the differential evolution technique. Acta Crystallogr B. 2002 Oct;58:823-34. doi: 10.1107/s0108768102011928. Epub 2002 Sep 24. PMID: 12324695.
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Micellar solutions of sulfobetaine surfactants in water-ethylene glycol mixtures: surface tension, fluorescence, spectroscopic, conductometric, and kinetic studies.

Langmuir : the ACS journal of surfaces and colloids

del Mar Graciani M, Rodríguez A, Muñoz M, Moyá ML.
PMID: 16042437
Langmuir. 2005 Aug 02;21(16):7161-9. doi: 10.1021/la050862j.

Micellization in water-ethylene glycol (EG) N-dodecyl, N-tetradecyl, and N-hexadecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate (SB3-12, SB3-14, and SB3-16, respectively) micellar solutions, with the weight percent of EG changing within the range 0-40, was studied by means of surface tension measurements. Information about the influence...

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del Mar Graciani M, Rodríguez A, Muñoz M, et al. Micellar solutions of sulfobetaine surfactants in water-ethylene glycol mixtures: surface tension, fluorescence, spectroscopic, conductometric, and kinetic studies. Langmuir. 2005;21(16):7161-9doi: 10.1021/la050862j.
del Mar Graciani, M., Rodríguez, A., Muñoz, M., & Moyá, M. L. (2005). Micellar solutions of sulfobetaine surfactants in water-ethylene glycol mixtures: surface tension, fluorescence, spectroscopic, conductometric, and kinetic studies. Langmuir : the ACS journal of surfaces and colloids, 21(16), 7161-9. https://doi.org/10.1021/la050862j
del Mar Graciani, María, et al. "Micellar solutions of sulfobetaine surfactants in water-ethylene glycol mixtures: surface tension, fluorescence, spectroscopic, conductometric, and kinetic studies." Langmuir : the ACS journal of surfaces and colloids vol. 21,16 (2005): 7161-9. doi: https://doi.org/10.1021/la050862j
del Mar Graciani M, Rodríguez A, Muñoz M, Moyá ML. Micellar solutions of sulfobetaine surfactants in water-ethylene glycol mixtures: surface tension, fluorescence, spectroscopic, conductometric, and kinetic studies. Langmuir. 2005 Aug 02;21(16):7161-9. doi: 10.1021/la050862j. PMID: 16042437.
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Estimation of Free Radical Ionization Energies by the Kinetic Method and the Relationship between the Kinetic Method and the Hammett Equation.

Analytical chemistry

Chen G, Wong P, Cooks RG.
PMID: 21639290
Anal Chem. 1997 Sep 01;69(17):3641-5. doi: 10.1021/ac970470k.

Substituted 1,2-diphenylethanes undergo competitive dissociations upon electron ionization (EI) to generate substituted benzyl cation and benzyl radical pairs. Application of the kinetic method to the previous reported EI mass spectra of these covalently bound precursor ions (data are taken...

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Chen G, Wong P, Cooks RG. Estimation of Free Radical Ionization Energies by the Kinetic Method and the Relationship between the Kinetic Method and the Hammett Equation. Anal Chem. 1997;69(17):3641-5doi: 10.1021/ac970470k.
Chen, G., Wong, P., & Cooks, R. G. (1997). Estimation of Free Radical Ionization Energies by the Kinetic Method and the Relationship between the Kinetic Method and the Hammett Equation. Analytical chemistry, 69(17), 3641-5. https://doi.org/10.1021/ac970470k
Chen, G, et al. "Estimation of Free Radical Ionization Energies by the Kinetic Method and the Relationship between the Kinetic Method and the Hammett Equation." Analytical chemistry vol. 69,17 (1997): 3641-5. doi: https://doi.org/10.1021/ac970470k
Chen G, Wong P, Cooks RG. Estimation of Free Radical Ionization Energies by the Kinetic Method and the Relationship between the Kinetic Method and the Hammett Equation. Anal Chem. 1997 Sep 01;69(17):3641-5. doi: 10.1021/ac970470k. PMID: 21639290.
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Identification of a novel biomarker for oxidative stress induced by hydrogen peroxide in primary human hepatocytes using the 2-nitrobenzenesulfenyl chloride isotope labeling method.

Hepatology research : the official journal of the Japan Society of Hepatology

Takami Y, Uto H, Tamai T, Sato Y, Ishida Y, Morinaga H, Sakakibara Y, Moriuchi A, Oketani M, Ido A, Nakajima T, Okanoue T, Tsubouchi H.
PMID: 20236361
Hepatol Res. 2010 Apr;40(4):438-45. doi: 10.1111/j.1872-034X.2009.00615.x. Epub 2010 Mar 07.

AIM: Oxidative stress is involved in the progression of non-alcoholic steatohepatitis (NASH). However, there are few biomarkers that are easily measured and accurately reflect the disease states. The aim of this study was to identify novel oxidative stress markers...

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Takami Y, Uto H, Tamai T, et al. Identification of a novel biomarker for oxidative stress induced by hydrogen peroxide in primary human hepatocytes using the 2-nitrobenzenesulfenyl chloride isotope labeling method. Hepatol Res. 2010;40(4):438-45doi: 10.1111/j.1872-034X.2009.00615.x.
Takami, Y., Uto, H., Tamai, T., Sato, Y., Ishida, Y., Morinaga, H., Sakakibara, Y., Moriuchi, A., Oketani, M., Ido, A., Nakajima, T., Okanoue, T., & Tsubouchi, H. (2010). Identification of a novel biomarker for oxidative stress induced by hydrogen peroxide in primary human hepatocytes using the 2-nitrobenzenesulfenyl chloride isotope labeling method. Hepatology research : the official journal of the Japan Society of Hepatology, 40(4), 438-45. https://doi.org/10.1111/j.1872-034X.2009.00615.x
Takami, Yoichiro, et al. "Identification of a novel biomarker for oxidative stress induced by hydrogen peroxide in primary human hepatocytes using the 2-nitrobenzenesulfenyl chloride isotope labeling method." Hepatology research : the official journal of the Japan Society of Hepatology vol. 40,4 (2010): 438-45. doi: https://doi.org/10.1111/j.1872-034X.2009.00615.x
Takami Y, Uto H, Tamai T, Sato Y, Ishida Y, Morinaga H, Sakakibara Y, Moriuchi A, Oketani M, Ido A, Nakajima T, Okanoue T, Tsubouchi H. Identification of a novel biomarker for oxidative stress induced by hydrogen peroxide in primary human hepatocytes using the 2-nitrobenzenesulfenyl chloride isotope labeling method. Hepatol Res. 2010 Apr;40(4):438-45. doi: 10.1111/j.1872-034X.2009.00615.x. Epub 2010 Mar 07. PMID: 20236361.
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Two dominant factors influencing the impact sensitivities of nitrobenzenes and saturated nitro compounds.

The journal of physical chemistry. B

Cao C, Gao S.
PMID: 17927238
J Phys Chem B. 2007 Nov 01;111(43):12399-402. doi: 10.1021/jp074078e. Epub 2007 Oct 10.

The factors governing the impact sensitivity (H(50)) of nitrobenzenes and saturated nitro compounds were studied. It was observed that the oxygen balances (OB(100)) and nitro group charge (Q(NO2)) are two important factors influencing the stability of these nitro compounds....

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Cao C, Gao S. Two dominant factors influencing the impact sensitivities of nitrobenzenes and saturated nitro compounds. J Phys Chem B. 2007;111(43):12399-402doi: 10.1021/jp074078e.
Cao, C., & Gao, S. (2007). Two dominant factors influencing the impact sensitivities of nitrobenzenes and saturated nitro compounds. The journal of physical chemistry. B, 111(43), 12399-402. https://doi.org/10.1021/jp074078e
Cao, Chenzhong, and Gao, Shuo. "Two dominant factors influencing the impact sensitivities of nitrobenzenes and saturated nitro compounds." The journal of physical chemistry. B vol. 111,43 (2007): 12399-402. doi: https://doi.org/10.1021/jp074078e
Cao C, Gao S. Two dominant factors influencing the impact sensitivities of nitrobenzenes and saturated nitro compounds. J Phys Chem B. 2007 Nov 01;111(43):12399-402. doi: 10.1021/jp074078e. Epub 2007 Oct 10. PMID: 17927238.
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Showing 1 to 12 of 132 entries