<p>Cobalt(II) dithiocarbazate-silane complex [3APTES + AQSMDTC@Co(II) complex] was synthesized using a newly developed Schiff base (SB) ligand derived from acenaphthoquinone (AQ), S-methyldithiocarbazate (MDTC), and (3-aminopropyl)triethoxysilane (3APTES), together with cobalt(II) acetate salt. The Co(II)-MSNs [MCM 41@AQSMDTC@Co(II) complex] was fabricated by MCM 41 on the cobalt(II) dithiocarbazate-silane complex. The new confirmation of the complex was extensively characterized using various analytical techniques. FT-IR was used to confirm the formation of thione-thiol, while SEM-EDX was employed to assess surface morphology and elemental composition. TEM analyses revealed a hexagonal morphology and an average particle size distribution of 14&#xa0;nm for MCM-41 and 12&#xa0;nm for the Co(II)-MSNs complex. PXRD was utilized to identify the 2θ reflections corresponding to d<sub>100</sub>, d<sub>110</sub>, and d<sub>200</sub>. Additionally, TGA indicated that the residue mass of MCM-41 is 89 wt%, while the Co(II)-MSNs complex has a residue mass of 88.5 wt%. N<sub>2</sub> absorption-desorption measurements showed that Co(II)-MSNs have a surface area of 411&#xa0;m²/g, a pore volume of 0.213&#xa0;cm³/g, and a pore size of 13&#xa0;nm, compared to MCM-41. Additionally, the heterogeneous catalyst was monitored for catecholase (Cat-ox) activity using UV-Vis spectroscopy, which involves the conversion of 3,5-di-tert-butylcatechol (3,5-DTBC) to 3,5-di-tert-butylquinone (3,5-DTBQ). The Co(II)-MSNs could be recovered and reused without significantly losing their catalytic ability.</p>

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MCM 41 Functionalized Cobalt(II) Complex Bearing NNS Dithiocarbazate and Its Bio-relevant Catechol Oxidase Mimics

  • Palaniappan Manikandan,
  • Paranthaman Vijayan,
  • Manogaran Tamiliniyaa,
  • Muthusami Rubiga,
  • Arumugam Selvi,
  • Rangappan Rajavel,
  • Tamilselvan Silambarasan,
  • Chandramohan Govindasamy,
  • Khalid M. Almutairi,
  • Santhosh Shanthi Bhupathi

摘要

Cobalt(II) dithiocarbazate-silane complex [3APTES + AQSMDTC@Co(II) complex] was synthesized using a newly developed Schiff base (SB) ligand derived from acenaphthoquinone (AQ), S-methyldithiocarbazate (MDTC), and (3-aminopropyl)triethoxysilane (3APTES), together with cobalt(II) acetate salt. The Co(II)-MSNs [MCM 41@AQSMDTC@Co(II) complex] was fabricated by MCM 41 on the cobalt(II) dithiocarbazate-silane complex. The new confirmation of the complex was extensively characterized using various analytical techniques. FT-IR was used to confirm the formation of thione-thiol, while SEM-EDX was employed to assess surface morphology and elemental composition. TEM analyses revealed a hexagonal morphology and an average particle size distribution of 14 nm for MCM-41 and 12 nm for the Co(II)-MSNs complex. PXRD was utilized to identify the 2θ reflections corresponding to d100, d110, and d200. Additionally, TGA indicated that the residue mass of MCM-41 is 89 wt%, while the Co(II)-MSNs complex has a residue mass of 88.5 wt%. N2 absorption-desorption measurements showed that Co(II)-MSNs have a surface area of 411 m²/g, a pore volume of 0.213 cm³/g, and a pore size of 13 nm, compared to MCM-41. Additionally, the heterogeneous catalyst was monitored for catecholase (Cat-ox) activity using UV-Vis spectroscopy, which involves the conversion of 3,5-di-tert-butylcatechol (3,5-DTBC) to 3,5-di-tert-butylquinone (3,5-DTBQ). The Co(II)-MSNs could be recovered and reused without significantly losing their catalytic ability.