Synthesis, XRD, spectral (IR, UV-Vis, NMR) characterization and quantum chemical exploration of benzoimidazole-based hydrazones: A synergistic experimental-computational analysis

Autor(es)

Rafiq, Muhammad ^[1] ; Khalid, Muhammad ^[2] ; Tahir, Muhammad Nawaz ^[3] ; Ahmad, Muhammad Umair ^[1] ; Khan, Muhammad Usman ^[4] ; Naseer, Muhammad Moazzam ^[5] ; Carmo Braga, Ataualpa Albert ^[6] ; Muhammad, Shabbir ^[7] ; Shafiq, Zahid ^[1]

Afiliação do(s) autor(es)

^[1] Bahauddin Zakariya Univ, Inst Chem Sci, Multan 60800 - Pakistan

^[2] Khwaja Fareed Univ Engn & Informat Technol, Dept Chem, Rahim Yar Khan 64200 - Pakistan

^[3] Univ Sargodha, Dept Phys, Sargodha 40100 - Pakistan

^[4] Govt Coll Univ, Dept Appl Chem, Faisalabad 38000 - Pakistan

^[5] Quaid I Azam Univ, Dept Chem, Islamabad 45320 - Pakistan

^[6] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, Ave Prof LineuPrestes 748, BR-05508000 Sao Paulo - Brazil

^[7] King Khalid Univ, Dept Phys, Coll Sci, POB 9004, Abha 61413 - Saudi Arabia

• Tipo de documento: Artigo Científico
• Fonte: Applied Organometallic Chemistry; v. 33, n. 11 AUG 2019.
• Citações Web of Science: 14

Resumo

Present study advocates the joint experimental and computational studies of two potent benzoimidazole-based hydrazones with chemical formula C23H18F2N4O (5a) and C25H22FN5O3 (5b). Both 5a and 5b were synthesized and resolved into their crystal structures using SC-XRD for the assessment of bond lengths, bond angles, unit cells and space groups. The structures of 5a and 5b were chemically characterized using infrared (FT-IR), UV-Visible, nuclear magnetic resonance (H-1-NMR and C-13-NMR), EIMS and elemental analysis. DFT at M06-2X/6-31G(d,p) level of theory was performed to get optimized structures and countercheck the experimental findings. Overall, DFT findings show excellent concurrence with the experimental data which confirms the purity of both compounds. FMO, NBO analysis, MEP surfaces and nonlinear optical (NLO) properties were explored at same level of theory. UV-Vis analysis at TDDFT/M06-2X/6-31G(d,p) level of theory showed that 5b is red shifted with lambda(max) 331.69 nm as compared to 5a with lambda(max) 240.25 nm. Global reactivity parameters were estimated using energy of FMOs indicated the greater harness value than the softness values of 5a and 5b. NBO analysis confirmed that the presence of non-covalent interactions, hydrogen bonding and hyper conjugative interactions are pivotal cause for the existence of 5a and 5b in the solid-state. NLO results of 5a and 5b were observed better than standard molecule recommended the NLO activity of said molecules for optoelectronic applications. (AU)

• Processo FAPESP: 11/07895-8 - Estudo teórico das reações de Heck-Matsuda
• Beneficiário: Ataualpa Albert Carmo Braga
• Linha de fomento: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 14/25770-6 - Novas fronteiras em reações de acoplamento cruzado mediadas por paládio: associando catálise enantiosseletiva, ativações C-H, novos materiais e reações em fluxo visando alta eficiência e sustentabilidade em processos sintéticos
• Beneficiário: Carlos Roque Duarte Correia
• Linha de fomento: Auxílio à Pesquisa - Temático
• Processo FAPESP: 15/01491-3 - Estudo teórico das reações de acoplamento-cruzado: catálise homogênea e heterogênea
• Beneficiário: Ataualpa Albert Carmo Braga
• Linha de fomento: Auxílio à Pesquisa - Regular