Synthesis, Spectroscopic Characterization, Thermogravimetric and Biological Activity Evaluation of Te(Ⅳ), Se(Ⅳ), V(Ⅲ), Nb(Ⅴ), Ta(Ⅴ) Complexes With Indole-3-Acetic Acid Plant Hormone Ligand
Synthesis, Spectroscopic Characterization, Thermogravimetric and Biological Activity Evaluation of Te(Ⅳ), Se(Ⅳ), V(Ⅲ), Nb(Ⅴ), Ta(Ⅴ) Complexes With Indole-3-Acetic Acid Plant Hormone Ligand
图 & 表
图 1.
Fig. 1. Structure of indole-3-acetic acid (IAAH)
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图 2.
Fig. 2. Suggested structures of IAA complexes
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图 3.
Fig. 3. FTIR spectra of IAA complexes Ⅰ—Ⅴ
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图 4.
Fig. 4. TG-DrTGA curve of [V(IAA)2(NH3)(Cl)] complex
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图 5.
Fig. 5. XRD pattern of IAA complexes Ⅰ—Ⅴ
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图 6.
Fig. 6. TEM images of (Ⅰ): tellurium and (Ⅳ): niobium complexes
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图 7.
Fig. 7. SEM images of IAA complexes Ⅰ—Ⅴ
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表 1Micro analytical and physical data of IAA complexes
Table1. Micro analytical and physical data of IAA complexes
Complex | Color | Magnetic moment (BM) | Conductance/ (ohm-1·cm2·mol-1) | Element | Calc. | Found |
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Ⅰ | Orange red | - | 96 | %C | 41.35 | 41.12 | %H | 3.82 | 3.77 | %N | 9.64 | 9.65 | %Cl | 12.21 | 12.09 | Ⅱ | Orange | - | 105 | %C | 45.13 | 45.03 | %H | 4.17 | 4.03 | %N | 10.53 | 10.45 | %Cl | 13.32 | 13.21 | Ⅲ | Olive green | 1.11 | 14 | %C | 53.17 | 53.06 | %H | 4.24 | 4.11 | %N | 9.30 | 9.23 | %Cl | 7.85 | 7.70 | Ⅳ | Yellow | - | 10 | %C | 43.87 | 43.65 | %H | 2.94 | 2.88 | %N | 5.12 | 5.06 | %Cl | 19.42 | 19.35 | Ⅴ | Yellow | - | 12 | %C | 37.79 | 37.81 | %H | 2.54 | 2.43 | %N | 4.41 | 4.38 | %Cl | 16.73 | 16.60 |
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表 2Infrared spectral data (cm-1) of IAA complexes Ⅰ—Ⅴ
Table2. Infrared spectral data (cm-1) of IAA complexes Ⅰ—Ⅴ
Compounds | Frequencies/cm-1 |
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ν(N—H) | νas(COO) | νs(COO) | ν(M—O) | ν(M—N) |
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I | 3 400 | 1 549 | 1 403 | 585, 517 | 429 | Ⅱ | 3 400 | 1 550 | 1 403 | 517 | 429 | Ⅲ | 3 400 | 1 549 | 1 403 | 595, 517 | 419 | Ⅳ | 3 390 | 1 549 | 1 403 | 634 | - | Ⅴ | 3 400 | 1 549 | 1 403 | 624 | - |
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表 31HNMR spectral data (cm-1) of IAA and its complexes (Ⅰ, Ⅱ, Ⅳ, and Ⅴ)
Table3. 1HNMR spectral data (cm-1) of IAA and its complexes (Ⅰ, Ⅱ, Ⅳ, and Ⅴ)
Assignments | Compounds |
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IAAH | Ⅰ | Ⅱ | Ⅳ | Ⅴ |
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1H, COOH | 12.16 | - | - | - | - | 1H, NH | 10.91 | 10.909 | 11.100 | 10.909 | 10.948 | 5H, C6H4, C=CH | 7.51~6.97 | 6.914~7.485 | 7.473 | 7.292 | 6.945~7.481 | 2H, CH2 | 3.64 | 3.721 | 3.434 | 3.353 | 3.728 |
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表 4Inhibition zone diameter of IAA complexes Ⅰ—Ⅴ against four bacterial strains
Table4. Inhibition zone diameter of IAA complexes Ⅰ—Ⅴ against four bacterial strains
sample | Inhibition zone diameter (mm·mg-1 sample) |
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Klebsiella | Esherichia Coli | Staphylococcus Epidermidis | Staphylococcus Aureus |
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Control: DMSO | 0.0 | 0.0 | 0.0 | 0.0 | Standard | Ceftriaxone Gentamycin | 0.0 0.3 | 0.0 0.0 | 1.6 1.8 | 1.9 1.5 | Ⅰ | 0.2 | 0.0 | 0.0 | 0.0 | Ⅱ | 0.1 | 0.0 | 0.0 | 0.0 | Ⅲ | 0.2 | 0.0 | 0.0 | 0.0 | Ⅳ | 0.1 | 0.0 | 0.0 | 0.0 | Ⅴ | 0.1 | 0.0 | 0.0 | 0.0 |
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, , , , . Synthesis, Spectroscopic Characterization, Thermogravimetric and Biological Activity Evaluation of Te(Ⅳ), Se(Ⅳ), V(Ⅲ), Nb(Ⅴ), Ta(Ⅴ) Complexes With Indole-3-Acetic Acid Plant Hormone Ligand[J]. 光谱学与光谱分析, 2021, 41(2): 658. Y. Al-Humaidi Jehan, A. Al-Saif Foziah, N. Binjawhar Dalal, A. Bakhsh Hanan, S. Refat Moamen. Synthesis, Spectroscopic Characterization, Thermogravimetric and Biological Activity Evaluation of Te(Ⅳ), Se(Ⅳ), V(Ⅲ), Nb(Ⅴ), Ta(Ⅴ) Complexes With Indole-3-Acetic Acid Plant Hormone Ligand[J]. Spectroscopy and Spectral Analysis, 2021, 41(2): 658.