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  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS

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      ASAD, Mohammad et al. Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies. Journal of Molecular Structure, v. 1201, p. 1-14 art. 127186, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2019.127186. Acesso em: 12 out. 2024.
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      Asad, M., Arshad, M. N., Khan, S. A., Oves, M., Khalid, M., Asiri, A. M., & Braga, A. A. C. (2020). Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies. Journal of Molecular Structure, 1201, 1-14 art. 127186. doi:10.1016/j.molstruc.2019.127186
    • NLM

      Asad M, Arshad MN, Khan SA, Oves M, Khalid M, Asiri AM, Braga AAC. Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies [Internet]. Journal of Molecular Structure. 2020 ; 1201 1-14 art. 127186.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127186
    • Vancouver

      Asad M, Arshad MN, Khan SA, Oves M, Khalid M, Asiri AM, Braga AAC. Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies [Internet]. Journal of Molecular Structure. 2020 ; 1201 1-14 art. 127186.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127186
  • Source: Dyes and Pigments. Unidades: IQ, FCF

    Subjects: SELÊNIO, PALÁDIO, FLUORESCÊNCIA

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      PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 12 out. 2024.
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      Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
    • NLM

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
    • Vancouver

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: DIFRAÇÃO POR RAIOS X, BENZENO, QUÍMICA DE COORDENAÇÃO

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      KHAN, Ezzat et al. Molecular structure of 1,4-bis(substituted-carbonyl)benzene: a combined experimental and theoretical approach. Journal of Molecular Structure, v. 1205, p. 1-14 art. 127633, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2019.127633. Acesso em: 12 out. 2024.
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      Khan, E., Khalid, M., Gul, Z., Shahzad, A., Tahir, M. N., Asif, H. M., et al. (2020). Molecular structure of 1,4-bis(substituted-carbonyl)benzene: a combined experimental and theoretical approach. Journal of Molecular Structure, 1205, 1-14 art. 127633. doi:10.1016/j.molstruc.2019.127633
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      Khan E, Khalid M, Gul Z, Shahzad A, Tahir MN, Asif HM, Asim S, Braga AAC. Molecular structure of 1,4-bis(substituted-carbonyl)benzene: a combined experimental and theoretical approach [Internet]. Journal of Molecular Structure. 2020 ; 1205 1-14 art. 127633.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127633
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      Khan E, Khalid M, Gul Z, Shahzad A, Tahir MN, Asif HM, Asim S, Braga AAC. Molecular structure of 1,4-bis(substituted-carbonyl)benzene: a combined experimental and theoretical approach [Internet]. Journal of Molecular Structure. 2020 ; 1205 1-14 art. 127633.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127633
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: ESPECTROSCOPIA, REAGENTES

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      BUENO, Marco A et al. A new piperazine: spectroscopic and theoretical conformational studies. Journal of Molecular Structure, v. 1203, n. 5, p. 1-5 art. 127420, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2019.127420. Acesso em: 12 out. 2024.
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      Bueno, M. A., Moura, R. G., Franco, M. P., Braga, A. A. C., Di Vitta, C., & Marzorati, L. (2020). A new piperazine: spectroscopic and theoretical conformational studies. Journal of Molecular Structure, 1203( 5), 1-5 art. 127420. doi:10.1016/j.molstruc.2019.127420
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      Bueno MA, Moura RG, Franco MP, Braga AAC, Di Vitta C, Marzorati L. A new piperazine: spectroscopic and theoretical conformational studies [Internet]. Journal of Molecular Structure. 2020 ; 1203( 5): 1-5 art. 127420.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127420
    • Vancouver

      Bueno MA, Moura RG, Franco MP, Braga AAC, Di Vitta C, Marzorati L. A new piperazine: spectroscopic and theoretical conformational studies [Internet]. Journal of Molecular Structure. 2020 ; 1203( 5): 1-5 art. 127420.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127420
  • Source: ARKIVOC - Archive for Organic Chemistry. Unidades: IQ, IQSC

    Subjects: QUÍMICA ORGÂNICA, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      OLIVEIRA, Marcelo Tavares de et al. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, p. 113-122, 2020Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.135. Acesso em: 12 out. 2024.
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      Oliveira, M. T. de, Alves, J. M. A., Morais, S. F. de A., & Braga, A. A. C. (2020). Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, 113-122. doi:10.24820/ark.5550190.p011.135
    • NLM

      Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2024 out. 12 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
    • Vancouver

      Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2024 out. 12 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
  • Source: Theoretical Chemistry Accounts. Unidades: FFCLRP, IQ

    Subjects: LIGANTES, ESCÂNDIO, COMPOSTOS HETEROCÍCLICOS

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      BATISTA, Ana Paula de Lima e OLIVEIRA FILHO, Antonio Gustavo Sampaio de. Probing N-heterocyclic olefin as ancillary ligand in scandium-mediated CO2 to CO conversion. Theoretical Chemistry Accounts, v. 139, p. 1-8 art. 42, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00214-019-2528-9. Acesso em: 12 out. 2024.
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      Batista, A. P. de L., & Oliveira Filho, A. G. S. de. (2020). Probing N-heterocyclic olefin as ancillary ligand in scandium-mediated CO2 to CO conversion. Theoretical Chemistry Accounts, 139, 1-8 art. 42. doi:10.1007/s00214-019-2528-9
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      Batista AP de L, Oliveira Filho AGS de. Probing N-heterocyclic olefin as ancillary ligand in scandium-mediated CO2 to CO conversion [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-8 art. 42.[citado 2024 out. 12 ] Available from: https://doi.org/10.1007/s00214-019-2528-9
    • Vancouver

      Batista AP de L, Oliveira Filho AGS de. Probing N-heterocyclic olefin as ancillary ligand in scandium-mediated CO2 to CO conversion [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-8 art. 42.[citado 2024 out. 12 ] Available from: https://doi.org/10.1007/s00214-019-2528-9
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: DIFRAÇÃO POR RAIOS X, ANÁLISE DE FOURIER

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      KHALID, Muhammad et al. O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation. Journal of Molecular Structure, v. 1224, p. 1-11 art. 129308, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129308. Acesso em: 12 out. 2024.
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      Khalid, M., Ali, A., Haq, S., Tahir, M. N., Iqbal, J., Braga, A. A. C., et al. (2020). O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation. Journal of Molecular Structure, 1224, 1-11 art. 129308. doi:10.1016/j.molstruc.2020.129308
    • NLM

      Khalid M, Ali A, Haq S, Tahir MN, Iqbal J, Braga AAC, Ashfaq M, Akhtar SUH. O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation [Internet]. Journal of Molecular Structure. 2020 ; 1224 1-11 art. 129308.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129308
    • Vancouver

      Khalid M, Ali A, Haq S, Tahir MN, Iqbal J, Braga AAC, Ashfaq M, Akhtar SUH. O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation [Internet]. Journal of Molecular Structure. 2020 ; 1224 1-11 art. 129308.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129308
  • Source: ACS Omega. Unidade: IQ

    Subjects: QUÍMICA QUÂNTICA, CROMO

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      RABIA BASRI, et al. Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis. ACS Omega, v. 5, n. 46, p. 30176–30188, 2020Tradução . . Disponível em: https://doi.org/10.1021/acsomega.0c04653. Acesso em: 12 out. 2024.
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      Rabia Basri,, Khalid, M., Shafiq, Z., Tahir, M. S., Khan, M. U., Tahir, M. N., et al. (2020). Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis. ACS Omega, 5( 46), 30176–30188. doi:10.1021/acsomega.0c04653
    • NLM

      Rabia Basri, Khalid M, Shafiq Z, Tahir MS, Khan MU, Tahir MN, Naseer MM, Braga AAC. Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis [Internet]. ACS Omega. 2020 ; 5( 46): 30176–30188.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c04653
    • Vancouver

      Rabia Basri, Khalid M, Shafiq Z, Tahir MS, Khan MU, Tahir MN, Naseer MM, Braga AAC. Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis [Internet]. ACS Omega. 2020 ; 5( 46): 30176–30188.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c04653
  • Source: Journal of Raman Spectroscopy. Unidade: IQ

    Subjects: NANOPARTÍCULAS, CARBONO, OURO, ESPECTROSCOPIA RAMAN

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      ROCHA, Júlio César da et al. Room temperature synthesis and Raman spectral evidence of carbon bond ranelate–gold nanoparticles. Journal of Raman Spectroscopy, v. 51, p. 1083–1091, 2020Tradução . . Disponível em: https://doi.org/10.1002/jrs.5872. Acesso em: 12 out. 2024.
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      Rocha, J. C. da, Mattioni, J. V., Sihn, L. M., Shinohara, J. da S., Melo, F. M. de, Franco, M. P., et al. (2020). Room temperature synthesis and Raman spectral evidence of carbon bond ranelate–gold nanoparticles. Journal of Raman Spectroscopy, 51, 1083–1091. doi:10.1002/jrs.5872
    • NLM

      Rocha JC da, Mattioni JV, Sihn LM, Shinohara J da S, Melo FM de, Franco MP, Braga AAC, Toma HE. Room temperature synthesis and Raman spectral evidence of carbon bond ranelate–gold nanoparticles [Internet]. Journal of Raman Spectroscopy. 2020 ; 51 1083–1091.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/jrs.5872
    • Vancouver

      Rocha JC da, Mattioni JV, Sihn LM, Shinohara J da S, Melo FM de, Franco MP, Braga AAC, Toma HE. Room temperature synthesis and Raman spectral evidence of carbon bond ranelate–gold nanoparticles [Internet]. Journal of Raman Spectroscopy. 2020 ; 51 1083–1091.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/jrs.5872
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: PALÁDIO, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      AKRAM, Muhammad et al. Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies. Journal of Molecular Structure, v. 1213, p. 1-15 art. 128131, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.128131. Acesso em: 12 out. 2024.
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      Akram, M., Adeel, M., Khalid, M., Tahir, M. N., Aliabad, H. A. R., Ullah, M. A., et al. (2020). Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies. Journal of Molecular Structure, 1213, 1-15 art. 128131. doi:10.1016/j.molstruc.2020.128131
    • NLM

      Akram M, Adeel M, Khalid M, Tahir MN, Aliabad HAR, Ullah MA, Iqbal J, Braga AAC. Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1213 1-15 art. 128131.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128131
    • Vancouver

      Akram M, Adeel M, Khalid M, Tahir MN, Aliabad HAR, Ullah MA, Iqbal J, Braga AAC. Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1213 1-15 art. 128131.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128131
  • Source: Advanced Synthesis and Catalysis. Unidade: IQ

    Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO

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      POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 12 out. 2024.
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      Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471
    • NLM

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/adsc.201901471
    • Vancouver

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/adsc.201901471
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: SULFONAMIDAS, INFECÇÕES BACTERIANAS, ALDEÍDOS

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      ARSHAD, Muhammad Nadeem et al. A potent synthesis and supramolecular synthon hierarchy percipience of (E)-Nʹ-(Napthalen-1-yl-methylene)-benzenesulfonohydrazide and 1-Napthaldehyde: A combined experimental and DFT studies. Journal of Molecular Structure, v. 1221, p. 1-8 art. 128797, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.128797. Acesso em: 12 out. 2024.
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      Arshad, M. N., Hussain, M. M., Asiri, A. M., Khalid, M., Braga, A. A. C., & Rahman, M. M. (2020). A potent synthesis and supramolecular synthon hierarchy percipience of (E)-Nʹ-(Napthalen-1-yl-methylene)-benzenesulfonohydrazide and 1-Napthaldehyde: A combined experimental and DFT studies. Journal of Molecular Structure, 1221, 1-8 art. 128797. doi:10.1016/j.molstruc.2020.128797
    • NLM

      Arshad MN, Hussain MM, Asiri AM, Khalid M, Braga AAC, Rahman MM. A potent synthesis and supramolecular synthon hierarchy percipience of (E)-Nʹ-(Napthalen-1-yl-methylene)-benzenesulfonohydrazide and 1-Napthaldehyde: A combined experimental and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1221 1-8 art. 128797.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128797
    • Vancouver

      Arshad MN, Hussain MM, Asiri AM, Khalid M, Braga AAC, Rahman MM. A potent synthesis and supramolecular synthon hierarchy percipience of (E)-Nʹ-(Napthalen-1-yl-methylene)-benzenesulfonohydrazide and 1-Napthaldehyde: A combined experimental and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1221 1-8 art. 128797.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128797
  • Source: Applied Organometallic Chemistry. Unidade: IQ

    Subjects: SULFONAMIDAS, METAIS

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      SUMRRA, Sajjad H et al. Synthesis, characterization, and biological screening of metal complexes of novel sulfonamide derivatives: experimental and theoretical analysis of sulfonamide crystal. Applied Organometallic Chemistry, v. 2020, p. 1-19 art. e5623 : + Supplementary materials ( S1-S9), 2020Tradução . . Disponível em: https://doi.org/10.1002/aoc.5623. Acesso em: 12 out. 2024.
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      Sumrra, S. H., Hassan, A. U., Imran, M., Khalid, M., Mughal, E. U., Zafar, M. N., et al. (2020). Synthesis, characterization, and biological screening of metal complexes of novel sulfonamide derivatives: experimental and theoretical analysis of sulfonamide crystal. Applied Organometallic Chemistry, 2020, 1-19 art. e5623 : + Supplementary materials ( S1-S9). doi:10.1002/aoc.5623
    • NLM

      Sumrra SH, Hassan AU, Imran M, Khalid M, Mughal EU, Zafar MN, Tahir MN, Raza MA, Braga AAC. Synthesis, characterization, and biological screening of metal complexes of novel sulfonamide derivatives: experimental and theoretical analysis of sulfonamide crystal [Internet]. Applied Organometallic Chemistry. 2020 ; 2020 1-19 art. e5623 : + Supplementary materials ( S1-S9).[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/aoc.5623
    • Vancouver

      Sumrra SH, Hassan AU, Imran M, Khalid M, Mughal EU, Zafar MN, Tahir MN, Raza MA, Braga AAC. Synthesis, characterization, and biological screening of metal complexes of novel sulfonamide derivatives: experimental and theoretical analysis of sulfonamide crystal [Internet]. Applied Organometallic Chemistry. 2020 ; 2020 1-19 art. e5623 : + Supplementary materials ( S1-S9).[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/aoc.5623
  • Source: Applied Organometallic Chemistry. Unidade: IQ

    Subjects: PALÁDIO, LIGANTES

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      CHEN, Ming-Tsz et al. N ,N ′-bridged binuclear NHC palladium complexes: A combined experimental catalytic and computational study for the Suzuki reaction. Applied Organometallic Chemistry, p. 1-16 art. e5870, 2020Tradução . . Disponível em: https://doi.org/10.1002/aoc.5870. Acesso em: 12 out. 2024.
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      Chen, M. -T., Hsieh, B. -Y., Liu, Y. -H., Lu, K. -H., Lussari, N., & Braga, A. A. C. (2020). N ,N ′-bridged binuclear NHC palladium complexes: A combined experimental catalytic and computational study for the Suzuki reaction. Applied Organometallic Chemistry, 1-16 art. e5870. doi:10.1002/aoc.5870
    • NLM

      Chen M-T, Hsieh B-Y, Liu Y-H, Lu K-H, Lussari N, Braga AAC. N ,N ′-bridged binuclear NHC palladium complexes: A combined experimental catalytic and computational study for the Suzuki reaction [Internet]. Applied Organometallic Chemistry. 2020 ; 1-16 art. e5870.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/aoc.5870
    • Vancouver

      Chen M-T, Hsieh B-Y, Liu Y-H, Lu K-H, Lussari N, Braga AAC. N ,N ′-bridged binuclear NHC palladium complexes: A combined experimental catalytic and computational study for the Suzuki reaction [Internet]. Applied Organometallic Chemistry. 2020 ; 1-16 art. e5870.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/aoc.5870
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: SAIS, ÁCIDOS

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      HANIF, Muhammad et al. 2-Amino-3-methylpyridinium, 2-amino-4-methylbenzothiazolium and 2-amino-5-chloropyridinium salts. experimental and theoretical findings. Journal of Molecular Structure, v. 1222, p. 1-16 art. 128914, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.128914. Acesso em: 12 out. 2024.
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      Hanif, M., Khan, E., Tahir, M. N., Morais, S. F. de A., & Braga, A. A. C. (2020). 2-Amino-3-methylpyridinium, 2-amino-4-methylbenzothiazolium and 2-amino-5-chloropyridinium salts. experimental and theoretical findings. Journal of Molecular Structure, 1222, 1-16 art. 128914. doi:10.1016/j.molstruc.2020.128914
    • NLM

      Hanif M, Khan E, Tahir MN, Morais SF de A, Braga AAC. 2-Amino-3-methylpyridinium, 2-amino-4-methylbenzothiazolium and 2-amino-5-chloropyridinium salts. experimental and theoretical findings [Internet]. Journal of Molecular Structure. 2020 ; 1222 1-16 art. 128914.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128914
    • Vancouver

      Hanif M, Khan E, Tahir MN, Morais SF de A, Braga AAC. 2-Amino-3-methylpyridinium, 2-amino-4-methylbenzothiazolium and 2-amino-5-chloropyridinium salts. experimental and theoretical findings [Internet]. Journal of Molecular Structure. 2020 ; 1222 1-16 art. 128914.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128914
  • Source: ACS Omega. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA, COMPOSTOS HETEROCÍCLICOS

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      ALI, Akbar et al. An experimental and computational exploration on the electronic, spectroscopic, and reactivity properties of novel halo-functionalized hydrazones. ACS Omega, v. 5, p. 18907−18918, 2020Tradução . . Disponível em: https://doi.org/10.1021/acsomega.0c02128. Acesso em: 12 out. 2024.
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      Ali, A., Khalid, M., Anwar, F., Aabidin, H. Z. -U., Akhtar, M. N., Khan, M. U., et al. (2020). An experimental and computational exploration on the electronic, spectroscopic, and reactivity properties of novel halo-functionalized hydrazones. ACS Omega, 5, 18907−18918. doi:10.1021/acsomega.0c02128
    • NLM

      Ali A, Khalid M, Anwar F, Aabidin HZ-U, Akhtar MN, Khan MU, Braga AAC, Assiri MA, Imran M. An experimental and computational exploration on the electronic, spectroscopic, and reactivity properties of novel halo-functionalized hydrazones [Internet]. ACS Omega. 2020 ; 5 18907−18918.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c02128
    • Vancouver

      Ali A, Khalid M, Anwar F, Aabidin HZ-U, Akhtar MN, Khan MU, Braga AAC, Assiri MA, Imran M. An experimental and computational exploration on the electronic, spectroscopic, and reactivity properties of novel halo-functionalized hydrazones [Internet]. ACS Omega. 2020 ; 5 18907−18918.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c02128
  • Source: Sensors & Actuators B. Unidade: IQ

    Subjects: ELETROANÁLISE, AMINAS

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      COUTO, Rosa A. S et al. Methylone screening with electropolymerized molecularly imprinted polymer on screen-printed electrodes. Sensors & Actuators B, v. 316, p. 1-10 art. 128133, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.snb.2020.128133. Acesso em: 12 out. 2024.
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      Couto, R. A. S., Mounssef Junior, B., Carvalho, F., Rodrigues, C. M. P., Braga, A. A. C., Aldous, L., et al. (2020). Methylone screening with electropolymerized molecularly imprinted polymer on screen-printed electrodes. Sensors & Actuators B, 316, 1-10 art. 128133. doi:10.1016/j.snb.2020.128133
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      Couto RAS, Mounssef Junior B, Carvalho F, Rodrigues CMP, Braga AAC, Aldous L, Gonçalves LM, Quinaz MB. Methylone screening with electropolymerized molecularly imprinted polymer on screen-printed electrodes [Internet]. Sensors & Actuators B. 2020 ; 316 1-10 art. 128133.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.snb.2020.128133
    • Vancouver

      Couto RAS, Mounssef Junior B, Carvalho F, Rodrigues CMP, Braga AAC, Aldous L, Gonçalves LM, Quinaz MB. Methylone screening with electropolymerized molecularly imprinted polymer on screen-printed electrodes [Internet]. Sensors & Actuators B. 2020 ; 316 1-10 art. 128133.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.snb.2020.128133
  • Source: Theoretical Chemistry Accounts. Unidade: IQ

    Subjects: CATÁLISE, LIGANTES

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      SILVA, Vitor Hugo Menezes da et al. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations. Theoretical Chemistry Accounts, v. 139, p. 1-13 art. 77, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00214-020-02588-x. Acesso em: 12 out. 2024.
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      Silva, V. H. M. da, Oliveira, C. C., Correia, C. R. D., & Braga, A. A. C. (2020). Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations. Theoretical Chemistry Accounts, 139, 1-13 art. 77. doi:10.1007/s00214-020-02588-x
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      Silva VHM da, Oliveira CC, Correia CRD, Braga AAC. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-13 art. 77.[citado 2024 out. 12 ] Available from: https://doi.org/10.1007/s00214-020-02588-x
    • Vancouver

      Silva VHM da, Oliveira CC, Correia CRD, Braga AAC. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-13 art. 77.[citado 2024 out. 12 ] Available from: https://doi.org/10.1007/s00214-020-02588-x
  • Source: ACS Omega. Unidade: IQ

    Subjects: COMPOSTOS AROMÁTICOS, COMPOSTOS ORGÂNICOS

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      ALI, Arif et al. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network. ACS Omega, v. 5, p. 15115−15128, 2020Tradução . . Disponível em: https://doi.org/10.1021/acsomega.0c00975. Acesso em: 12 out. 2024.
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      Ali, A., Khalid, M., Rehman, M. F. ur, Haq, S., Ali, A., Tahir, M. N., et al. (2020). Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network. ACS Omega, 5, 15115−15128. doi:10.1021/acsomega.0c00975
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      Ali A, Khalid M, Rehman MF ur, Haq S, Ali A, Tahir MN, Ashfaq M, Rasool F, Braga AAC. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network [Internet]. ACS Omega. 2020 ; 5 15115−15128.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c00975
    • Vancouver

      Ali A, Khalid M, Rehman MF ur, Haq S, Ali A, Tahir MN, Ashfaq M, Rasool F, Braga AAC. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network [Internet]. ACS Omega. 2020 ; 5 15115−15128.[citado 2024 out. 12 ] Available from: https://doi.org/10.1021/acsomega.0c00975
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: DIFRAÇÃO POR RAIOS X, ALCALOIDES

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      TARIQ, Sobia et al. Synthesis and structural analysis of novel indole derivatives by XRD, spectroscopic and DFT studies. Journal of Molecular Structure, v. 1203, p. 1-15 art. 127438, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2019.127438. Acesso em: 12 out. 2024.
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      Tariq, S., Raza, A. R., Khalid, M., Rubab, S. L., Khan, M. U., Ali, A., et al. (2020). Synthesis and structural analysis of novel indole derivatives by XRD, spectroscopic and DFT studies. Journal of Molecular Structure, 1203, 1-15 art. 127438. doi:10.1016/j.molstruc.2019.127438
    • NLM

      Tariq S, Raza AR, Khalid M, Rubab SL, Khan MU, Ali A, Tahir MN, Braga AAC. Synthesis and structural analysis of novel indole derivatives by XRD, spectroscopic and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1203 1-15 art. 127438.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127438
    • Vancouver

      Tariq S, Raza AR, Khalid M, Rubab SL, Khan MU, Ali A, Tahir MN, Braga AAC. Synthesis and structural analysis of novel indole derivatives by XRD, spectroscopic and DFT studies [Internet]. Journal of Molecular Structure. 2020 ; 1203 1-15 art. 127438.[citado 2024 out. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127438

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