ReP USP - Resultado da busca

Artigo de periodico
Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network (2021)
Khalid, Muhammad ; Ali, Akbar ; Khan, Muhammad Usman ; Tahir, Muhammad Nawaz; Ahmad, Anees ; Ashfaq, Muhammad; Hussain, Riaz; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Source: Journal of Molecular Structure. Unidades: IQ, IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 30 jun. 2024.
APA
Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827
NLM
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Vancouver
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Artigo de periodico
Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule (2021)
Grothe, Renata A ; Lobato, Alnilan Cristina Barros ; Mounssef Junior, Bassim ; Tasić, Nikola ; Braga, Ataualpa Albert Carmo ; Maldaner, Adriano Otavio ; Aldous, Leigh ; Paixão, Thiago Regis Longo Cesar da ; Gonçalves, Luís Moreira
Source: Analyst. Unidade: IQ
Subjects: COCAÍNA, ANESTÉSICOS, VOLTAMETRIA, ELETROANÁLISE
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ABNT
GROTHE, Renata A et al. Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule. Analyst, v. 146, n. 5, p. 747-1759 : + Supplementary materials ( S1-S42), 2021Tradução . . Disponível em: https://doi.org/10.1039/d0an02274h. Acesso em: 30 jun. 2024.
APA
Grothe, R. A., Lobato, A. C. B., Mounssef Junior, B., Tasić, N., Braga, A. A. C., Maldaner, A. O., et al. (2021). Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule. Analyst, 146( 5), 747-1759 : + Supplementary materials ( S1-S42). doi:10.1039/d0an02274h
NLM
Grothe RA, Lobato ACB, Mounssef Junior B, Tasić N, Braga AAC, Maldaner AO, Aldous L, Paixão TRLC da, Gonçalves LM. Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule [Internet]. Analyst. 2021 ; 146( 5): 747-1759 : + Supplementary materials ( S1-S42).[citado 2024 jun. 30 ] Available from: https://doi.org/10.1039/d0an02274h
Vancouver
Grothe RA, Lobato ACB, Mounssef Junior B, Tasić N, Braga AAC, Maldaner AO, Aldous L, Paixão TRLC da, Gonçalves LM. Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule [Internet]. Analyst. 2021 ; 146( 5): 747-1759 : + Supplementary materials ( S1-S42).[citado 2024 jun. 30 ] Available from: https://doi.org/10.1039/d0an02274h
Artigo de periodico
A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach (2021)
Pasha, Anam Rubbab; Khalid, Muhammad; Shafiq, Zahid; Khan, Muhammad Usman; Naseer, Muhammad Moazzam; Tahir, Muhammad Nawaz; Hussain, Riaz; Braga, Ataualpa Albert Carmo ; Jawaria, Rifat
Source: Journal of Molecular Structure. Unidade: IQ
Assunto: COMPOSTOS HETEROCÍCLICOS
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PASHA, Anam Rubbab et al. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach. Journal of Molecular Structure, v. 1230, p. 1-11 art. 129852, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129852. Acesso em: 30 jun. 2024.
APA
Pasha, A. R., Khalid, M., Shafiq, Z., Khan, M. U., Naseer, M. M., Tahir, M. N., et al. (2021). A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach. Journal of Molecular Structure, 1230, 1-11 art. 129852. doi:10.1016/j.molstruc.2020.129852
NLM
Pasha AR, Khalid M, Shafiq Z, Khan MU, Naseer MM, Tahir MN, Hussain R, Braga AAC, Jawaria R. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach [Internet]. Journal of Molecular Structure. 2021 ; 1230 1-11 art. 129852.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129852
Vancouver
Pasha AR, Khalid M, Shafiq Z, Khan MU, Naseer MM, Tahir MN, Hussain R, Braga AAC, Jawaria R. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach [Internet]. Journal of Molecular Structure. 2021 ; 1230 1-11 art. 129852.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129852
Artigo de periodico
3,4-Methylenedioxypyrovalerone (MDPV) sensing based on electropolymerized molecularly imprinted polymers on silver nanoparticles and carboxylated multi-walled carbon nanotubes (2021)
Couto, Rosa A. S ; Coelho, Constantino; Mounssef Junior, Bassim; Morais, Sara Figueirêdo de Alcântara ; Lima, Camila D; Santos, Wallans Torres Pio dos ; Carvalho, Félix ; Rodrigues, Cecília M. P ; Braga, Ataualpa Albert Carmo ; Gonçalves, Luís Moreira ; Quinaz, M. Beatriz
Source: Nanomaterials. Unidade: IQ
Subjects: NANOTUBOS, NANOPARTÍCULAS, PRATA, CARBONO, QUÍMICA ANALÍTICA, QUÍMICA FORÊNSICA
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ABNT
COUTO, Rosa A. S et al. 3,4-Methylenedioxypyrovalerone (MDPV) sensing based on electropolymerized molecularly imprinted polymers on silver nanoparticles and carboxylated multi-walled carbon nanotubes. Nanomaterials, v. 11, p. 1-18 art. 353 : + Supplementary materials ( S1-S5), 2021Tradução . . Disponível em: https://doi.org/10.3390/nano11020353. Acesso em: 30 jun. 2024.
APA
Couto, R. A. S., Coelho, C., Mounssef Junior, B., Morais, S. F. de A., Lima, C. D., Santos, W. T. P. dos, et al. (2021). 3,4-Methylenedioxypyrovalerone (MDPV) sensing based on electropolymerized molecularly imprinted polymers on silver nanoparticles and carboxylated multi-walled carbon nanotubes. Nanomaterials, 11, 1-18 art. 353 : + Supplementary materials ( S1-S5). doi:10.3390/nano11020353
NLM
Couto RAS, Coelho C, Mounssef Junior B, Morais SF de A, Lima CD, Santos WTP dos, Carvalho F, Rodrigues CMP, Braga AAC, Gonçalves LM, Quinaz MB. 3,4-Methylenedioxypyrovalerone (MDPV) sensing based on electropolymerized molecularly imprinted polymers on silver nanoparticles and carboxylated multi-walled carbon nanotubes [Internet]. Nanomaterials. 2021 ; 11 1-18 art. 353 : + Supplementary materials ( S1-S5).[citado 2024 jun. 30 ] Available from: https://doi.org/10.3390/nano11020353
Vancouver
Couto RAS, Coelho C, Mounssef Junior B, Morais SF de A, Lima CD, Santos WTP dos, Carvalho F, Rodrigues CMP, Braga AAC, Gonçalves LM, Quinaz MB. 3,4-Methylenedioxypyrovalerone (MDPV) sensing based on electropolymerized molecularly imprinted polymers on silver nanoparticles and carboxylated multi-walled carbon nanotubes [Internet]. Nanomaterials. 2021 ; 11 1-18 art. 353 : + Supplementary materials ( S1-S5).[citado 2024 jun. 30 ] Available from: https://doi.org/10.3390/nano11020353
Artigo de periodico
Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)
Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Source: Dyes and Pigments. Unidades: IQ, FCF
Subjects: SELÊNIO, PALÁDIO, FLUORESCÊNCIA
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Artigo de periodico
A new piperazine: spectroscopic and theoretical conformational studies (2020)
Bueno, Marco A; Moura, Rebeca Garcia ; Franco, Maurício Portiolli ; Braga, Ataualpa Albert Carmo ; Di Vitta, Cláudio ; Marzorati, Liliana
Source: Journal of Molecular Structure. Unidade: IQ
Subjects: ESPECTROSCOPIA, REAGENTES
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ABNT
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: 30 jun. 2024.
APA
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
NLM
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127420
Artigo de periodico
Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds (2020)
Oliveira, Marcelo Tavares de; Alves, Júlia Maria Aragon; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Source: ARKIVOC - Archive for Organic Chemistry. Unidades: IQ, IQSC
Subjects: QUÍMICA ORGÂNICA, RESSONÂNCIA MAGNÉTICA NUCLEAR
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
Artigo de periodico
O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation (2020)
Khalid, Muhammad ; Ali, Akbar; Haq, Sadia; Tahir, Muhammad Nawaz; Iqbal, Javed; Braga, Ataualpa Albert Carmo ; Ashfaq, Muhammad; Akhtar, Samee Ul Hassan
Source: Journal of Molecular Structure. Unidade: IQ
Subjects: DIFRAÇÃO POR RAIOS X, ANÁLISE DE FOURIER
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129308
Artigo de periodico
Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis (2020)
Rabia Basri; Khalid, Muhammad ; Shafiq, Zahid ; Tahir, Muhammad Suleman; Khan, Muhammad Usman; Tahir, Muhammad Nawaz; Naseer, Muhammad Moazzam; Braga, Ataualpa Albert Carmo
Source: ACS Omega. Unidade: IQ
Subjects: QUÍMICA QUÂNTICA, CROMO
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1021/acsomega.0c04653
Artigo de periodico
Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies (2020)
Akram, Muhammad; Adeel, Muhammad; Khalid, Muhammad ; Tahir, Muhammad Nawaz; Aliabad, Hossein Asghar Rahnamaye; Ullah, Malik Aman; Iqbal, Javed; Braga, Ataualpa Albert Carmo
Source: Journal of Molecular Structure. Unidade: IQ
Subjects: PALÁDIO, RESSONÂNCIA MAGNÉTICA NUCLEAR
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128131
Artigo de periodico
Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity (2020)
Polo, Ellen Christine; Wang, Martí Fernández; Angnes, Ricardo Almir; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Advanced Synthesis and Catalysis. Unidade: IQ
Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1002/adsc.201901471
Artigo de periodico
N ,N ′-bridged binuclear NHC palladium complexes: A combined experimental catalytic and computational study for the Suzuki reaction (2020)
Chen, Ming-Tsz ; Hsieh, Bing-Yan; Liu, Yi-Hung; Lu, Kuo-Hui; Lussari, Natália ; Braga, Ataualpa Albert Carmo
Source: Applied Organometallic Chemistry. Unidade: IQ
Subjects: PALÁDIO, LIGANTES
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1002/aoc.5870
Artigo de periodico
Methylone screening with electropolymerized molecularly imprinted polymer on screen-printed electrodes (2020)
Couto, Rosa A. S; Mounssef Junior, Bassim; Carvalho, Félix; Rodrigues, Cecília M. P; Braga, Ataualpa Albert Carmo ; Aldous, Leigh; Gonçalves, Luís Moreira ; Quinaz, M. Beatriz
Source: Sensors & Actuators B. Unidade: IQ
Subjects: ELETROANÁLISE, AMINAS
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ABNT
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: 30 jun. 2024.
APA
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
NLM
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.snb.2020.128133
Artigo de periodico
Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network (2020)
Ali, Arif; Khalid, Muhammad; Rehman, Muhammad Fayyaz ur ; Haq, Sadia; Ali, Arif; Tahir, Muhammad Nawaz; Ashfaq, Muhammad; Rasool, Faiz; Braga, Ataualpa Albert Carmo
Source: ACS Omega. Unidade: IQ
Subjects: COMPOSTOS AROMÁTICOS, COMPOSTOS ORGÂNICOS
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ABNT
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: 30 jun. 2024.
APA
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
NLM
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1021/acsomega.0c00975
Artigo de periodico
Synthesis and structural analysis of novel indole derivatives by XRD, spectroscopic and DFT studies (2020)
Tariq, Sobia; Raza, Abdul Rauf; Khalid, Muhammad; Rubab, Syeda Laila; Khan, Muhammad Usman; Ali, Akbar; Tahir, Muhammad Nawaz; Braga, Ataualpa Albert Carmo
Source: Journal of Molecular Structure. Unidade: IQ
Subjects: DIFRAÇÃO POR RAIOS X, ALCALOIDES
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ABNT
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: 30 jun. 2024.
APA
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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.molstruc.2019.127438
Artigo de periodico
A facile microwave assisted synthesis and structure elucidation of (3R)-3-alkyl-4,1-benzoxazepine-2,5-diones by crystallographic, spectroscopic and DFT studies (2020)
Raza, Abdul Rauf; Nisar, Bushra; Khalid, Muhammad ; Gondal, Humaira Yasmeen; Khan, Muhammad Usman ; Morais, Sara Figueirêdo de Alcântara ; Tahir, Muhammad Nawaz; Braga, Ataualpa Albert Carmo
Source: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. Unidade: IQ
Subjects: TECNOLOGIA DE MICRO-ONDAS, IRRADIAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAZA, Abdul Rauf et al. A facile microwave assisted synthesis and structure elucidation of (3R)-3-alkyl-4,1-benzoxazepine-2,5-diones by crystallographic, spectroscopic and DFT studies. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v. 230, p. 1-15 art. 117995, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2019.117995. Acesso em: 30 jun. 2024.
APA
Raza, A. R., Nisar, B., Khalid, M., Gondal, H. Y., Khan, M. U., Morais, S. F. de A., et al. (2020). A facile microwave assisted synthesis and structure elucidation of (3R)-3-alkyl-4,1-benzoxazepine-2,5-diones by crystallographic, spectroscopic and DFT studies. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 230, 1-15 art. 117995. doi:10.1016/j.saa.2019.117995
NLM
Raza AR, Nisar B, Khalid M, Gondal HY, Khan MU, Morais SF de A, Tahir MN, Braga AAC. A facile microwave assisted synthesis and structure elucidation of (3R)-3-alkyl-4,1-benzoxazepine-2,5-diones by crystallographic, spectroscopic and DFT studies [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2020 ; 230 1-15 art. 117995.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.saa.2019.117995
Vancouver
Raza AR, Nisar B, Khalid M, Gondal HY, Khan MU, Morais SF de A, Tahir MN, Braga AAC. A facile microwave assisted synthesis and structure elucidation of (3R)-3-alkyl-4,1-benzoxazepine-2,5-diones by crystallographic, spectroscopic and DFT studies [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2020 ; 230 1-15 art. 117995.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.saa.2019.117995
Artigo de periodico
Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: a synergistic experimental-computational analysis (2019)
Rafiq, Muhammad; Khalid, Muhammad ; Tahir, Muhammad Nawaz; Ahmad, Muhammad Umair; Khan, Muhammad Usman; Naseer, Muhammad Moazzam; Braga, Ataualpa Albert Carmo ; Muhammad, Shabbir; Shafiq, Zahid
Source: Applied Organometallic Chemistry. Unidade: IQ
Subjects: QUÍMICA QUÂNTICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAFIQ, Muhammad et al. Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: a synergistic experimental-computational analysis. Applied Organometallic Chemistry, v. 33, p. 1-17 art. e5182, 2019Tradução . . Disponível em: https://doi.org/10.1002/aoc.5182. Acesso em: 30 jun. 2024.
APA
Rafiq, M., Khalid, M., Tahir, M. N., Ahmad, M. U., Khan, M. U., Naseer, M. M., et al. (2019). Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: a synergistic experimental-computational analysis. Applied Organometallic Chemistry, 33, 1-17 art. e5182. doi:10.1002/aoc.5182
NLM
Rafiq M, Khalid M, Tahir MN, Ahmad MU, Khan MU, Naseer MM, Braga AAC, Muhammad S, Shafiq Z. Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: a synergistic experimental-computational analysis [Internet]. Applied Organometallic Chemistry. 2019 ; 33 1-17 art. e5182.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1002/aoc.5182
Vancouver
Rafiq M, Khalid M, Tahir MN, Ahmad MU, Khan MU, Naseer MM, Braga AAC, Muhammad S, Shafiq Z. Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: a synergistic experimental-computational analysis [Internet]. Applied Organometallic Chemistry. 2019 ; 33 1-17 art. e5182.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1002/aoc.5182
Tese (Doutorado)
Estudo teórico de reações enantiosseletivas de morita-baylis-hillman: o efeito da base hatakeyama (2019)
Nascimento, Verônica Maria do; Braga, Ataualpa Albert Carmo (Orientador)
Unidade: IQ
Subjects: REAÇÕES QUÍMICAS, REAÇÕES ORGÂNICAS
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ABNT
NASCIMENTO, Verônica Maria do. Estudo teórico de reações enantiosseletivas de morita-baylis-hillman: o efeito da base hatakeyama. 2019. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2019. Disponível em: https://www.teses.usp.br/teses/disponiveis/46/46136/tde-09032020-144444/. Acesso em: 30 jun. 2024.
APA
Nascimento, V. M. do. (2019). Estudo teórico de reações enantiosseletivas de morita-baylis-hillman: o efeito da base hatakeyama (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de https://www.teses.usp.br/teses/disponiveis/46/46136/tde-09032020-144444/
NLM
Nascimento VM do. Estudo teórico de reações enantiosseletivas de morita-baylis-hillman: o efeito da base hatakeyama [Internet]. 2019 ;[citado 2024 jun. 30 ] Available from: https://www.teses.usp.br/teses/disponiveis/46/46136/tde-09032020-144444/
Vancouver
Nascimento VM do. Estudo teórico de reações enantiosseletivas de morita-baylis-hillman: o efeito da base hatakeyama [Internet]. 2019 ;[citado 2024 jun. 30 ] Available from: https://www.teses.usp.br/teses/disponiveis/46/46136/tde-09032020-144444/
Artigo de periodico
DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts (2019)
Silva, Vitor Hugo Menezes da ; Morgon, Nelson H ; Correia, Carlos R. D ; Braga, Ataualpa Albert Carmo
Source: Journal of Organometallic Chemistry. Unidade: IQ
Subjects: REAÇÕES QUÍMICAS, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Vitor Hugo Menezes da et al. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, v. 896, p. 5-15, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2019.05.023. Acesso em: 30 jun. 2024.
APA
Silva, V. H. M. da, Morgon, N. H., Correia, C. R. D., & Braga, A. A. C. (2019). DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, 896, 5-15. doi:10.1016/j.jorganchem.2019.05.023
NLM
Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
Vancouver
Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
Artigo de periodico
Electrochemical sensing of ecstasy with electropolymerized molecularly imprinted poly(o-phenylenediamine) polymer on the surface of disposable screen-printed carbon electrodes (2019)
Couto, Rosa A. S; Costa, Séfora S; Mounssef Junior, Bassim; Pacheco, João G; Fernandes, Eduarda; Carvalho, Félix; Rodrigues, Cecília M. P; Matos, Cristina Delerue; Braga, Ataualpa Albert Carmo ; Gonçalves, Luís Moreira ; Quinaz, M. Beatriz
Source: Sensors and Actuators B. Unidade: IQ
Subjects: ELETROQUÍMICA, GEOMETRIA E MODELAGEM COMPUTACIONAL, ELETROANÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTO, Rosa A. S et al. Electrochemical sensing of ecstasy with electropolymerized molecularly imprinted poly(o-phenylenediamine) polymer on the surface of disposable screen-printed carbon electrodes. Sensors and Actuators B, v. 290, n. 1, p. 378-386, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.snb.2019.03.138. Acesso em: 30 jun. 2024.
APA
Couto, R. A. S., Costa, S. S., Mounssef Junior, B., Pacheco, J. G., Fernandes, E., Carvalho, F., et al. (2019). Electrochemical sensing of ecstasy with electropolymerized molecularly imprinted poly(o-phenylenediamine) polymer on the surface of disposable screen-printed carbon electrodes. Sensors and Actuators B, 290( 1), 378-386. doi:10.1016/j.snb.2019.03.138
NLM
Couto RAS, Costa SS, Mounssef Junior B, Pacheco JG, Fernandes E, Carvalho F, Rodrigues CMP, Matos CD, Braga AAC, Gonçalves LM, Quinaz MB. Electrochemical sensing of ecstasy with electropolymerized molecularly imprinted poly(o-phenylenediamine) polymer on the surface of disposable screen-printed carbon electrodes [Internet]. Sensors and Actuators B. 2019 ; 290( 1): 378-386.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.snb.2019.03.138
Vancouver
Couto RAS, Costa SS, Mounssef Junior B, Pacheco JG, Fernandes E, Carvalho F, Rodrigues CMP, Matos CD, Braga AAC, Gonçalves LM, Quinaz MB. Electrochemical sensing of ecstasy with electropolymerized molecularly imprinted poly(o-phenylenediamine) polymer on the surface of disposable screen-printed carbon electrodes [Internet]. Sensors and Actuators B. 2019 ; 290( 1): 378-386.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.snb.2019.03.138

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