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  • Source: Journal of the American Chemical Society. Unidades: IF, IQ

    Subjects: FOTOBIOLOGIA, ESPECTROSCOPIA

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      VALVERDE, Danillo et al. Ultrafast intersystem crossing dynamics of 6-selenoguanine in water. Journal of the American Chemical Society, v. 2, n. 7, p. 1699-1711, 2022Tradução . . Disponível em: https://doi.org/10.1021/jacsau.2c00250. Acesso em: 16 abr. 2024.
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      Valverde, D., Mai, S., Canuto, S. R. A., Borin, A. C., & González, L. (2022). Ultrafast intersystem crossing dynamics of 6-selenoguanine in water. Journal of the American Chemical Society, 2( 7), 1699-1711. doi:10.1021/jacsau.2c00250
    • NLM

      Valverde D, Mai S, Canuto SRA, Borin AC, González L. Ultrafast intersystem crossing dynamics of 6-selenoguanine in water [Internet]. Journal of the American Chemical Society. 2022 ; 2( 7): 1699-1711.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacsau.2c00250
    • Vancouver

      Valverde D, Mai S, Canuto SRA, Borin AC, González L. Ultrafast intersystem crossing dynamics of 6-selenoguanine in water [Internet]. Journal of the American Chemical Society. 2022 ; 2( 7): 1699-1711.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacsau.2c00250
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: CRISTALOGRAFIA, HIDROGÊNIO, HALOGÊNIOS

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      SURBELLA, Robert G et al. Transuranic hybrid materials: crystallographic and computational metrics of supramolecular assembly. Journal of the American Chemical Society, v. 139, n. 31, p. 10843-10855, 2017Tradução . . Disponível em: https://doi.org/10.1021/jacs.7b05689. Acesso em: 16 abr. 2024.
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      Surbella, R. G., Ducati, L. C., Pellegrini, K. L., McNamara, B. K., Autschbach, J., Schwantes, J. M., & Cahill, C. L. (2017). Transuranic hybrid materials: crystallographic and computational metrics of supramolecular assembly. Journal of the American Chemical Society, 139( 31), 10843-10855. doi:10.1021/jacs.7b05689
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      Surbella RG, Ducati LC, Pellegrini KL, McNamara BK, Autschbach J, Schwantes JM, Cahill CL. Transuranic hybrid materials: crystallographic and computational metrics of supramolecular assembly [Internet]. Journal of the American Chemical Society. 2017 ; 139( 31): 10843-10855.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.7b05689
    • Vancouver

      Surbella RG, Ducati LC, Pellegrini KL, McNamara BK, Autschbach J, Schwantes JM, Cahill CL. Transuranic hybrid materials: crystallographic and computational metrics of supramolecular assembly [Internet]. Journal of the American Chemical Society. 2017 ; 139( 31): 10843-10855.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.7b05689
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Assunto: QUÍMICA INORGÂNICA

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      ARCHUT, A et al. Toward photoswitchable dendritic hosts. Interaction between azobenzene-functionalized dendrimers and eosin. Journal of the American Chemical Society, v. 120, n. 47, p. 12187-12191, 1998Tradução . . Acesso em: 16 abr. 2024.
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      Archut, A., Azzellini, G. C., Balzani, V., De Cola, L., & Vögtle, F. (1998). Toward photoswitchable dendritic hosts. Interaction between azobenzene-functionalized dendrimers and eosin. Journal of the American Chemical Society, 120( 47), 12187-12191.
    • NLM

      Archut A, Azzellini GC, Balzani V, De Cola L, Vögtle F. Toward photoswitchable dendritic hosts. Interaction between azobenzene-functionalized dendrimers and eosin. Journal of the American Chemical Society. 1998 ; 120( 47): 12187-12191.[citado 2024 abr. 16 ]
    • Vancouver

      Archut A, Azzellini GC, Balzani V, De Cola L, Vögtle F. Toward photoswitchable dendritic hosts. Interaction between azobenzene-functionalized dendrimers and eosin. Journal of the American Chemical Society. 1998 ; 120( 47): 12187-12191.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: FFCLRP

    Assunto: QUÍMICA

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      CLIVE, D L J et al. Total synthesis of both (+) - compaction and (+) - mevinolin: a general strategy based on the use of a special ti'C IND.13' / 'C IND.8'k misture for dicarbonyl coupling. Journal of the American Chemical Society, v. 110, n. 20, p. 6914-6, 1988Tradução . . Acesso em: 16 abr. 2024.
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      Clive, D. L. J., Murthy, K. S. K., Wee, A. G. A., Prasad, J. S., Silva, G. V. J., Majewshi, M., et al. (1988). Total synthesis of both (+) - compaction and (+) - mevinolin: a general strategy based on the use of a special ti'C IND.13' / 'C IND.8'k misture for dicarbonyl coupling. Journal of the American Chemical Society, 110( 20), 6914-6.
    • NLM

      Clive DLJ, Murthy KSK, Wee AGA, Prasad JS, Silva GVJ, Majewshi M, Anderson PC, Haugen RD, Heerze LD. Total synthesis of both (+) - compaction and (+) - mevinolin: a general strategy based on the use of a special ti'C IND.13' / 'C IND.8'k misture for dicarbonyl coupling. Journal of the American Chemical Society. 1988 ;110( 20): 6914-6.[citado 2024 abr. 16 ]
    • Vancouver

      Clive DLJ, Murthy KSK, Wee AGA, Prasad JS, Silva GVJ, Majewshi M, Anderson PC, Haugen RD, Heerze LD. Total synthesis of both (+) - compaction and (+) - mevinolin: a general strategy based on the use of a special ti'C IND.13' / 'C IND.8'k misture for dicarbonyl coupling. Journal of the American Chemical Society. 1988 ;110( 20): 6914-6.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DERRICK, L et al. Total synthesis of both (+) - compactin and (+) - mevinolim. A general strategy based on the use of a special titanium regent for decarbonyl coupling. Journal of the American Chemical Society, v. 112, n. 8 , p. 3018-28, 1990Tradução . . Disponível em: https://doi.org/10.1021/ja00164a024. Acesso em: 16 abr. 2024.
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      Derrick, L., Clive, J., Keshava Murthy, K. S., Wee, A. G. H., Prasad, J. S., Silva, G. V. J., et al. (1990). Total synthesis of both (+) - compactin and (+) - mevinolim. A general strategy based on the use of a special titanium regent for decarbonyl coupling. Journal of the American Chemical Society, 112( 8 ), 3018-28. doi:10.1021/ja00164a024
    • NLM

      Derrick L, Clive J, Keshava Murthy KS, Wee AGH, Prasad JS, Silva GVJ, Majewski M, Anderson PC, Evans CF, Haugen RD, Heerze LD, Barrie JR. Total synthesis of both (+) - compactin and (+) - mevinolim. A general strategy based on the use of a special titanium regent for decarbonyl coupling [Internet]. Journal of the American Chemical Society. 1990 ;112( 8 ): 3018-28.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja00164a024
    • Vancouver

      Derrick L, Clive J, Keshava Murthy KS, Wee AGH, Prasad JS, Silva GVJ, Majewski M, Anderson PC, Evans CF, Haugen RD, Heerze LD, Barrie JR. Total synthesis of both (+) - compactin and (+) - mevinolim. A general strategy based on the use of a special titanium regent for decarbonyl coupling [Internet]. Journal of the American Chemical Society. 1990 ;112( 8 ): 3018-28.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja00164a024
  • Source: Journal of the American Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA

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      BOJES, J et al. The thio analogue of peroxynitrite, '[SSNS] POT.-: preparation, electronic structure, resonance raman spectrum, and formation of complexes with nickel and cobalt. Journal of the American Chemical Society, v. 102, n. 104, p. 4837-4841, 1982Tradução . . Disponível em: https://doi.org/10.1021/ja00382a017. Acesso em: 16 abr. 2024.
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      Bojes, J., Chivers, T., Laidlaw, W. G., & Trsic, M. (1982). The thio analogue of peroxynitrite, '[SSNS] POT.-: preparation, electronic structure, resonance raman spectrum, and formation of complexes with nickel and cobalt. Journal of the American Chemical Society, 102( 104), 4837-4841. doi:10.1021/ja00382a017
    • NLM

      Bojes J, Chivers T, Laidlaw WG, Trsic M. The thio analogue of peroxynitrite, '[SSNS] POT.-: preparation, electronic structure, resonance raman spectrum, and formation of complexes with nickel and cobalt [Internet]. Journal of the American Chemical Society. 1982 ; 102( 104): 4837-4841.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja00382a017
    • Vancouver

      Bojes J, Chivers T, Laidlaw WG, Trsic M. The thio analogue of peroxynitrite, '[SSNS] POT.-: preparation, electronic structure, resonance raman spectrum, and formation of complexes with nickel and cobalt [Internet]. Journal of the American Chemical Society. 1982 ; 102( 104): 4837-4841.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja00382a017
  • Source: Journal of the American Chemical Society. Unidade: IFSC

    Subjects: CRISTALOGRAFIA FÍSICA (ESTRUTURA), COBRE, LIGAÇÕES QUÍMICAS, ESPECTROSCOPIA (CARACTERÍSTICAS)

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      LEDESMA, Gabriela N. et al. The met axial ligand determines the redox potential in 'Cu IND. A' sites. Journal of the American Chemical Society, v. 129, n. 39, p. 11884-11885, 2007Tradução . . Acesso em: 16 abr. 2024.
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      Ledesma, G. N., Murgida, D. H., Hoang, K. L., Wackerbarth, H., Ulstrup, J., Costa Filho, A. J. da, & Vila, A. J. (2007). The met axial ligand determines the redox potential in 'Cu IND. A' sites. Journal of the American Chemical Society, 129( 39), 11884-11885.
    • NLM

      Ledesma GN, Murgida DH, Hoang KL, Wackerbarth H, Ulstrup J, Costa Filho AJ da, Vila AJ. The met axial ligand determines the redox potential in 'Cu IND. A' sites. Journal of the American Chemical Society. 2007 ; 129( 39): 11884-11885.[citado 2024 abr. 16 ]
    • Vancouver

      Ledesma GN, Murgida DH, Hoang KL, Wackerbarth H, Ulstrup J, Costa Filho AJ da, Vila AJ. The met axial ligand determines the redox potential in 'Cu IND. A' sites. Journal of the American Chemical Society. 2007 ; 129( 39): 11884-11885.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: BIOQUÍMICA, OXIDAÇÃO

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      MARTINEZ, Gláucia R et al. Synthesis of a naphthalene endoperoxide as a source of `ANTPOT. 18O-labeled singlet oxygen for mechanistic studies. Journal of the American Chemical Society, v. 122, n. 41, p. 10212-10213, 2000Tradução . . Acesso em: 16 abr. 2024.
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      Martinez, G. R., Ravanat, J. -L., Medeiros, M. H. G. de, Cadet, J., & Di Mascio, P. (2000). Synthesis of a naphthalene endoperoxide as a source of `ANTPOT. 18O-labeled singlet oxygen for mechanistic studies. Journal of the American Chemical Society, 122( 41), 10212-10213.
    • NLM

      Martinez GR, Ravanat J-L, Medeiros MHG de, Cadet J, Di Mascio P. Synthesis of a naphthalene endoperoxide as a source of `ANTPOT. 18O-labeled singlet oxygen for mechanistic studies. Journal of the American Chemical Society. 2000 ; 122( 41): 10212-10213.[citado 2024 abr. 16 ]
    • Vancouver

      Martinez GR, Ravanat J-L, Medeiros MHG de, Cadet J, Di Mascio P. Synthesis of a naphthalene endoperoxide as a source of `ANTPOT. 18O-labeled singlet oxygen for mechanistic studies. Journal of the American Chemical Society. 2000 ; 122( 41): 10212-10213.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Assunto: NANOTECNOLOGIA

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      ZHANG, Hui et al. Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction. Journal of the American Chemical Society, v. 133, n. 15, p. 6078-6089, 2011Tradução . . Disponível em: https://doi.org/10.1021/ja201156s. Acesso em: 16 abr. 2024.
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      Zhang, H., Jin, M., Wang, J., Li, W., Camargo, P. H. C. de, Kim, M. J., et al. (2011). Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction. Journal of the American Chemical Society, 133( 15), 6078-6089. doi:10.1021/ja201156s
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      Zhang H, Jin M, Wang J, Li W, Camargo PHC de, Kim MJ, Yang D, Xie Z, Xia Y. Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction [Internet]. Journal of the American Chemical Society. 2011 ; 133( 15): 6078-6089.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja201156s
    • Vancouver

      Zhang H, Jin M, Wang J, Li W, Camargo PHC de, Kim MJ, Yang D, Xie Z, Xia Y. Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction [Internet]. Journal of the American Chemical Society. 2011 ; 133( 15): 6078-6089.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/ja201156s
  • Source: Journal of the American Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA

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      CHIVERS, T et al. Synthesis and crystal and molecular structure of ['('Ph IND.3') IND.2''N POT.+'['S IND.4''N POT.-'] and the electronic structure of the planar acyclic anion, 'S IND.4''N POT.-1'. Journal of the American Chemical Society, v. 102, n. 18, p. 5773-5781, 1980Tradução . . Acesso em: 16 abr. 2024.
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      Chivers, T., Laidlaw, W. G., Oakley, R. T., & Trsic, M. (1980). Synthesis and crystal and molecular structure of ['('Ph IND.3') IND.2''N POT.+'['S IND.4''N POT.-'] and the electronic structure of the planar acyclic anion, 'S IND.4''N POT.-1'. Journal of the American Chemical Society, 102( 18), 5773-5781.
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      Chivers T, Laidlaw WG, Oakley RT, Trsic M. Synthesis and crystal and molecular structure of ['('Ph IND.3') IND.2''N POT.+'['S IND.4''N POT.-'] and the electronic structure of the planar acyclic anion, 'S IND.4''N POT.-1'. Journal of the American Chemical Society. 1980 ; 102( 18): 5773-5781.[citado 2024 abr. 16 ]
    • Vancouver

      Chivers T, Laidlaw WG, Oakley RT, Trsic M. Synthesis and crystal and molecular structure of ['('Ph IND.3') IND.2''N POT.+'['S IND.4''N POT.-'] and the electronic structure of the planar acyclic anion, 'S IND.4''N POT.-1'. Journal of the American Chemical Society. 1980 ; 102( 18): 5773-5781.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, COMPOSTOS ORGANOMETÁLICOS, ESTEREOQUÍMICA

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      MARINO, Joseph P. et al. Stereocontrolled synthesis of(-)-macrolactin A. Journal of the American Chemical Society, v. 124, n. 8, p. 1664-1668, 2002Tradução . . Disponível em: http://pubs.acs.org/journals/jacsat/article.cgi/jacsat/2002/124/i08/pdf/ja017177t.pdf. Acesso em: 16 abr. 2024.
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      Marino, J. P., McClure, M. S., Holub, D. P., Comasseto, J. V., & Tucci, F. C. (2002). Stereocontrolled synthesis of(-)-macrolactin A. Journal of the American Chemical Society, 124( 8), 1664-1668. Recuperado de http://pubs.acs.org/journals/jacsat/article.cgi/jacsat/2002/124/i08/pdf/ja017177t.pdf
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      Marino JP, McClure MS, Holub DP, Comasseto JV, Tucci FC. Stereocontrolled synthesis of(-)-macrolactin A [Internet]. Journal of the American Chemical Society. 2002 ; 124( 8): 1664-1668.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/journals/jacsat/article.cgi/jacsat/2002/124/i08/pdf/ja017177t.pdf
    • Vancouver

      Marino JP, McClure MS, Holub DP, Comasseto JV, Tucci FC. Stereocontrolled synthesis of(-)-macrolactin A [Internet]. Journal of the American Chemical Society. 2002 ; 124( 8): 1664-1668.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/journals/jacsat/article.cgi/jacsat/2002/124/i08/pdf/ja017177t.pdf
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: BIOQUÍMICA, ÁCIDOS GRAXOS, CROMATOGRAFIA

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      MIYAMOTO, Sayuri et al. Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using O-18-labeled linoleic acid hydroperoxide and monomol light emission measurements. Journal of the American Chemical Society, v. 125, n. 20, p. 6172-6179, 2003Tradução . . Acesso em: 16 abr. 2024.
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      Miyamoto, S., Martinez, G. R., Medeiros, M. H. G. de, & Di Mascio, P. (2003). Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using O-18-labeled linoleic acid hydroperoxide and monomol light emission measurements. Journal of the American Chemical Society, 125( 20), 6172-6179.
    • NLM

      Miyamoto S, Martinez GR, Medeiros MHG de, Di Mascio P. Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using O-18-labeled linoleic acid hydroperoxide and monomol light emission measurements. Journal of the American Chemical Society. 2003 ; 125( 20): 6172-6179.[citado 2024 abr. 16 ]
    • Vancouver

      Miyamoto S, Martinez GR, Medeiros MHG de, Di Mascio P. Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using O-18-labeled linoleic acid hydroperoxide and monomol light emission measurements. Journal of the American Chemical Society. 2003 ; 125( 20): 6172-6179.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: IFSC

    Assunto: QUÍMICA INORGÂNICA

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      NAMOR, Angela F Danil de et al. Selective interaction of lower rim calix[4] arene derivatives and bivalent cations on solution. Crystallographic evidence of the versatile behavior of the acetonitrile in lead(II) and cadmium(II) complexes. Journal of the American Chemical Society, v. 124, n. 43, p. 12824-12836, 2002Tradução . . Acesso em: 16 abr. 2024.
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      Namor, A. F. D. de, Chahine, S., Kowalska, D., Castellano, E. E., & Piro, O. E. (2002). Selective interaction of lower rim calix[4] arene derivatives and bivalent cations on solution. Crystallographic evidence of the versatile behavior of the acetonitrile in lead(II) and cadmium(II) complexes. Journal of the American Chemical Society, 124( 43), 12824-12836.
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      Namor AFD de, Chahine S, Kowalska D, Castellano EE, Piro OE. Selective interaction of lower rim calix[4] arene derivatives and bivalent cations on solution. Crystallographic evidence of the versatile behavior of the acetonitrile in lead(II) and cadmium(II) complexes. Journal of the American Chemical Society. 2002 ; 124( 43): 12824-12836.[citado 2024 abr. 16 ]
    • Vancouver

      Namor AFD de, Chahine S, Kowalska D, Castellano EE, Piro OE. Selective interaction of lower rim calix[4] arene derivatives and bivalent cations on solution. Crystallographic evidence of the versatile behavior of the acetonitrile in lead(II) and cadmium(II) complexes. Journal of the American Chemical Society. 2002 ; 124( 43): 12824-12836.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: CENA

    Subjects: QUÍMICA ANALÍTICA, ESPECTROSCOPIA

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      BOUBNOV, Alexey et al. Selective catalytic reduction of NO over Fe-ZSM-5: mechanistic insights by operando HERFD-XANES and valence-to-core X-ray emission spectroscopy. Journal of the American Chemical Society, v. 136, p. 13006−13015 2014, 2014Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ja5062505. Acesso em: 16 abr. 2024.
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      Boubnov, A., Carvalho, H. W. P. de, Doronkin, D. E., Günter, T., Gallo, E., Atkins, A. J., et al. (2014). Selective catalytic reduction of NO over Fe-ZSM-5: mechanistic insights by operando HERFD-XANES and valence-to-core X-ray emission spectroscopy. Journal of the American Chemical Society, 136, 13006−13015 2014. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ja5062505
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      Boubnov A, Carvalho HWP de, Doronkin DE, Günter T, Gallo E, Atkins AJ, Jacob CR, Grunwaldt J-D. Selective catalytic reduction of NO over Fe-ZSM-5: mechanistic insights by operando HERFD-XANES and valence-to-core X-ray emission spectroscopy [Internet]. Journal of the American Chemical Society. 2014 ; 136 13006−13015 2014.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ja5062505
    • Vancouver

      Boubnov A, Carvalho HWP de, Doronkin DE, Günter T, Gallo E, Atkins AJ, Jacob CR, Grunwaldt J-D. Selective catalytic reduction of NO over Fe-ZSM-5: mechanistic insights by operando HERFD-XANES and valence-to-core X-ray emission spectroscopy [Internet]. Journal of the American Chemical Society. 2014 ; 136 13006−13015 2014.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ja5062505
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Assunto: FÍSICO-QUÍMICA

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      QUINA, Frank Herbert. Resenha sem titulo proprio. Journal of the American Chemical Society. Washington: Instituto de Química, Universidade de São Paulo. . Acesso em: 16 abr. 2024. , 1989
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      Quina, F. H. (1989). Resenha sem titulo proprio. Journal of the American Chemical Society. Washington: Instituto de Química, Universidade de São Paulo.
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      Quina FH. Resenha sem titulo proprio. Journal of the American Chemical Society. 1989 ;111( 6 ): 2366.[citado 2024 abr. 16 ]
    • Vancouver

      Quina FH. Resenha sem titulo proprio. Journal of the American Chemical Society. 1989 ;111( 6 ): 2366.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidades: IFSC, IQSC

    Subjects: CRISTALOGRAFIA, FOTOQUÍMICA

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      CARLOS, Rose Maria et al. Reactivity of radicals generated on irradiation of trans-[Ru'(N'H IND.3')IND.4'(N'O IND.2')P'(OEt)IND.3](P'F IND.6). Journal of the American Chemical Society, v. 126, n. 8, p. 2546-2555, 2004Tradução . . Acesso em: 16 abr. 2024.
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      Carlos, R. M., Cardoso, D. R., Castellano, E. E., Osti, R. Z., Camargo, A. J., Macedo, L. G., & Franco, D. W. (2004). Reactivity of radicals generated on irradiation of trans-[Ru'(N'H IND.3')IND.4'(N'O IND.2')P'(OEt)IND.3](P'F IND.6). Journal of the American Chemical Society, 126( 8), 2546-2555.
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      Carlos RM, Cardoso DR, Castellano EE, Osti RZ, Camargo AJ, Macedo LG, Franco DW. Reactivity of radicals generated on irradiation of trans-[Ru'(N'H IND.3')IND.4'(N'O IND.2')P'(OEt)IND.3](P'F IND.6). Journal of the American Chemical Society. 2004 ; 126( 8): 2546-2555.[citado 2024 abr. 16 ]
    • Vancouver

      Carlos RM, Cardoso DR, Castellano EE, Osti RZ, Camargo AJ, Macedo LG, Franco DW. Reactivity of radicals generated on irradiation of trans-[Ru'(N'H IND.3')IND.4'(N'O IND.2')P'(OEt)IND.3](P'F IND.6). Journal of the American Chemical Society. 2004 ; 126( 8): 2546-2555.[citado 2024 abr. 16 ]
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: LIPÍDEOS, LIGAÇÕES QUÍMICAS

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      BACELLAR, Isabel de Oliveira Lima et al. Photosensitized membrane permeabilization requires contact-dependent Reactions between photosensitizer and lipids. Journal of the American Chemical Society, v. 140, p. 9606−9615, 2018Tradução . . Disponível em: https://doi.org/10.1021/jacs.8b05014. Acesso em: 16 abr. 2024.
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      Bacellar, I. de O. L., Oliveira, M. C., Dantas, L. S., Costa, E. B., Junqueira, H. C., Martins, W. K., et al. (2018). Photosensitized membrane permeabilization requires contact-dependent Reactions between photosensitizer and lipids. Journal of the American Chemical Society, 140, 9606−9615. doi:10.1021/jacs.8b05014
    • NLM

      Bacellar I de OL, Oliveira MC, Dantas LS, Costa EB, Junqueira HC, Martins WK, Durantini AM, Cosa G, Di Mascio P, Wainwright M, Miotto R, Cordeiro RM, Miyamoto S, Baptista M da S. Photosensitized membrane permeabilization requires contact-dependent Reactions between photosensitizer and lipids [Internet]. Journal of the American Chemical Society. 2018 ; 140 9606−9615.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.8b05014
    • Vancouver

      Bacellar I de OL, Oliveira MC, Dantas LS, Costa EB, Junqueira HC, Martins WK, Durantini AM, Cosa G, Di Mascio P, Wainwright M, Miotto R, Cordeiro RM, Miyamoto S, Baptista M da S. Photosensitized membrane permeabilization requires contact-dependent Reactions between photosensitizer and lipids [Internet]. Journal of the American Chemical Society. 2018 ; 140 9606−9615.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.8b05014
  • Source: Journal of the American Chemical Society. Unidade: IQSC

    Assunto: ESPECTROSCOPIA MOLECULAR

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      SANTOS, Willy Glen dos et al. Photoinduced charge shifts and electron transfer in viologen - traphensylborate complexes: push - pull character of the exciplex. Journal of the American Chemical Society, v. 139, n. 23, p. 7681-7684, 2017Tradução . . Disponível em: https://doi.org/10.1021/jacs.7b01946. Acesso em: 16 abr. 2024.
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      Santos, W. G. dos, Budkina, D. S., Deflon, V. M., Tarnovsky, A. N., Cardoso, D. R., & Forbes, M. D. E. (2017). Photoinduced charge shifts and electron transfer in viologen - traphensylborate complexes: push - pull character of the exciplex. Journal of the American Chemical Society, 139( 23), 7681-7684. doi:10.1021/jacs.7b01946
    • NLM

      Santos WG dos, Budkina DS, Deflon VM, Tarnovsky AN, Cardoso DR, Forbes MDE. Photoinduced charge shifts and electron transfer in viologen - traphensylborate complexes: push - pull character of the exciplex [Internet]. Journal of the American Chemical Society. 2017 ; 139( 23): 7681-7684.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.7b01946
    • Vancouver

      Santos WG dos, Budkina DS, Deflon VM, Tarnovsky AN, Cardoso DR, Forbes MDE. Photoinduced charge shifts and electron transfer in viologen - traphensylborate complexes: push - pull character of the exciplex [Internet]. Journal of the American Chemical Society. 2017 ; 139( 23): 7681-7684.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.7b01946
  • Source: Journal of the American Chemical Society. Unidade: IQ

    Subjects: FOTOQUÍMICA, OXIDAÇÃO

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      TASSO, Thiago Teixeira et al. Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers. Journal of the American Chemical Society, v. 141, n. 39, p. 15547-15556, 2019Tradução . . Disponível em: https://doi.org/10.1021/jacs.9b05991. Acesso em: 16 abr. 2024.
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      Tasso, T. T., Schlothauer, J. C., Junqueira, H. C., Matias, T. A., Araki, K., Salvador, E. L., et al. (2019). Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers. Journal of the American Chemical Society, 141( 39), 15547-15556. doi:10.1021/jacs.9b05991
    • NLM

      Tasso TT, Schlothauer JC, Junqueira HC, Matias TA, Araki K, Salvador EL, Antonio FCT, Mello PH de, Baptista M da S. Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers [Internet]. Journal of the American Chemical Society. 2019 ; 141( 39): 15547-15556.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.9b05991
    • Vancouver

      Tasso TT, Schlothauer JC, Junqueira HC, Matias TA, Araki K, Salvador EL, Antonio FCT, Mello PH de, Baptista M da S. Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers [Internet]. Journal of the American Chemical Society. 2019 ; 141( 39): 15547-15556.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1021/jacs.9b05991
  • Source: Journal of the American Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA

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      SCHNEIDER, Gregory F. et al. Pathway for unfolding of ubiquitin in sodium dodecyl sulfate, studied by capillary electrophoresis. Journal of the American Chemical Society, v. 130, n. 51, p. 17384-17393, 2008Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/ja804736t. Acesso em: 16 abr. 2024.
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      Schneider, G. F., Shaw, B. F., Lee, A., Carrilho, E., & Whitesides, G. M. (2008). Pathway for unfolding of ubiquitin in sodium dodecyl sulfate, studied by capillary electrophoresis. Journal of the American Chemical Society, 130( 51), 17384-17393. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/ja804736t
    • NLM

      Schneider GF, Shaw BF, Lee A, Carrilho E, Whitesides GM. Pathway for unfolding of ubiquitin in sodium dodecyl sulfate, studied by capillary electrophoresis [Internet]. Journal of the American Chemical Society. 2008 ; 130( 51): 17384-17393.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/ja804736t
    • Vancouver

      Schneider GF, Shaw BF, Lee A, Carrilho E, Whitesides GM. Pathway for unfolding of ubiquitin in sodium dodecyl sulfate, studied by capillary electrophoresis [Internet]. Journal of the American Chemical Society. 2008 ; 130( 51): 17384-17393.[citado 2024 abr. 16 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/ja804736t

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