Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized TUD-1: an efficient catalyst for immediate and quantitative epoxidation of cyclohexene under ambient conditions. (14th November 2020)
- Record Type:
- Journal Article
- Title:
- Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized TUD-1: an efficient catalyst for immediate and quantitative epoxidation of cyclohexene under ambient conditions. (14th November 2020)
- Main Title:
- Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized TUD-1: an efficient catalyst for immediate and quantitative epoxidation of cyclohexene under ambient conditions
- Authors:
- Abboud, Mohamed
Sahlabji, Taher
Eissa, Murad
Bel-Hadj-Tahar, Radhouane
Mubarak, Ahmed T.
Al-Zaqri, Nabil
Hamdy, Mohamed S. - Abstract:
- Abstract : Nickel(ii )dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized TUD-1 as a new nanocatalyst for spontaneous and quantitative epoxidation of cyclohexene under ambient conditions. Abstract : A nickel(ii )dibenzotetramethyltetraaza[14]annulene complex (Nitmtaa) is prepared and immobilized on amino-functionalized TUD-1 (N-TUD-1) via a Ni–N (NH2 ) bond to obtain a stable and reusable new nanocatalyst named as Nitmtaa@N-TUD-1. The catalytic activity performance of this new nanocatalyst was evaluated in the epoxidation of cyclohexene under ambient conditions (25 °C, 1 atm) using meta -chloroperoxybenzoic acid ( m -CPBA) as the oxidant, and CH2 Cl2 /CH3 CN (1 : 1 v/v) as the solvent. (3-Aminopropyl)triethoxysilane (APTES) was first grafted on the TUD-1 surface, then Nitmtaa was added and coordinated with amine groups on the TUD-1 surface to produce the nanocatalyst Nitmtaa@N-TUD-1. The structure and morphology of the obtained nanocatalyst were studied using SEM, HR-TEM, BET analysis, FTIR spectroscopy, and powder XRD analysis. The thermal stability was investigated using TGA and DTA. HR-TEM and XRD results revealed a high dispersion of Nitmtaa on the TUD-1 surface. The obtained nanocatalyst exhibited an immediate and quantitative epoxidation reaction of cyclohexene to cyclohexene oxide under ambient conditions with a high turnover frequency (TOF) of ∼42.11 s −1 . Moreover, the catalyst Nitmtaa@N-TUD-1 maintained the high catalytic activityAbstract : Nickel(ii )dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized TUD-1 as a new nanocatalyst for spontaneous and quantitative epoxidation of cyclohexene under ambient conditions. Abstract : A nickel(ii )dibenzotetramethyltetraaza[14]annulene complex (Nitmtaa) is prepared and immobilized on amino-functionalized TUD-1 (N-TUD-1) via a Ni–N (NH2 ) bond to obtain a stable and reusable new nanocatalyst named as Nitmtaa@N-TUD-1. The catalytic activity performance of this new nanocatalyst was evaluated in the epoxidation of cyclohexene under ambient conditions (25 °C, 1 atm) using meta -chloroperoxybenzoic acid ( m -CPBA) as the oxidant, and CH2 Cl2 /CH3 CN (1 : 1 v/v) as the solvent. (3-Aminopropyl)triethoxysilane (APTES) was first grafted on the TUD-1 surface, then Nitmtaa was added and coordinated with amine groups on the TUD-1 surface to produce the nanocatalyst Nitmtaa@N-TUD-1. The structure and morphology of the obtained nanocatalyst were studied using SEM, HR-TEM, BET analysis, FTIR spectroscopy, and powder XRD analysis. The thermal stability was investigated using TGA and DTA. HR-TEM and XRD results revealed a high dispersion of Nitmtaa on the TUD-1 surface. The obtained nanocatalyst exhibited an immediate and quantitative epoxidation reaction of cyclohexene to cyclohexene oxide under ambient conditions with a high turnover frequency (TOF) of ∼42.11 s −1 . Moreover, the catalyst Nitmtaa@N-TUD-1 maintained the high catalytic activity performance and exhibited high stability in four successive cycles. The atomic absorption spectroscopy (AAS) experiments performed on the filtrate after each cycle showed a negligible leaching of Nitmtaa from the support N-TUD-1. A plausible reaction mechanism pathway is also proposed. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 46(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 46(2020)
- Issue Display:
- Volume 44, Issue 46 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 46
- Issue Sort Value:
- 2020-0044-0046-0000
- Page Start:
- 20137
- Page End:
- 20147
- Publication Date:
- 2020-11-14
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d0nj03822a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15511.xml