INDEX [] · S1 Supporting information for Zirconium–MOF catalysed selective synthesis of α-...

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S1 Supporting information for Zirconium–MOF catalysed selective synthesis of α- hydroxyamide via transfer hydrogenation of α-ketoamide Ashish A. Mishra and Bhalchandra M. Bhanage * Department of Chemistry, Institute of Chemical Technology, Matunga, Mumbai-400019. India. Tel: +91 22 33612601; Fax: +91 22 33611020. E-mail: [email protected] ; [email protected] INDEX No. Characterization Analysed Page No. 1. Powder XRD of Catalyst S2 2. TGA-DTGA of Catalyst S3 3. FT-IR of Catalyst & Catalytic Recycle Study S4 4. 1 H & 13 C NMR of α-hydroxyl amide and its derivative S5 - S20 Electronic Supplementary Material (ESI) for New Journal of Chemistry. This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2019

Transcript of INDEX [] · S1 Supporting information for Zirconium–MOF catalysed selective synthesis of α-...

Page 1: INDEX [] · S1 Supporting information for Zirconium–MOF catalysed selective synthesis of α- hydroxyamide via transfer hydrogenation of α-ketoamide Ashish A. Mishra† and Bhalchandra

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Supporting informationfor

Zirconium–MOF catalysed selective synthesis of α-hydroxyamide via transfer hydrogenation of α-ketoamide

Ashish A. Mishra† and Bhalchandra M. Bhanage†*†Department of Chemistry, Institute of Chemical Technology, Matunga, Mumbai-400019. India.

Tel: +91 22 33612601; Fax: +91 22 33611020.

E-mail: [email protected] ; [email protected]

INDEXNo. Characterization Analysed Page No.

1. Powder XRD of Catalyst S2

2. TGA-DTGA of Catalyst S3

3. FT-IR of Catalyst & Catalytic Recycle Study S4

4. 1H & 13C NMR of α-hydroxyl amide and its derivative

S5 - S20

Electronic Supplementary Material (ESI) for New Journal of Chemistry.This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2019

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X-RAY DIFFRACTION OF UiO66 & UiO66-NH2

Figure 1: XRD pattern for UiO66

Figure 2: XRD pattern for UiO66-NH2

Figure 3: XRD pattern for UiO-66 fresh and 4th recyclable catalyst

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Thermogravimetric analysis

Figure 4: Thermogravimetric analysis of UiO66 and UiO66-NH2

Figure 5: Thermogravimetric analysis and DTA of UiO66-NH2

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Figure 6: Infra-Red Spectroscopy of UiO66 and UiO66-NH2

1 2 3 4 5102030405060708090

100

% Yield Recovered

Run Cycle

% Y

ield

of p

rodu

ct

Figure 7: Catalytic Cycle

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1H and 13C NMR of α-hydroxyamide and its derivative

500 MHz 1H-NMR spectra of 2a in DMSO-d6

126 MHz 13C-NMR spectra of 2a in DMSO-d6

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500 MHz 1H-NMR spectra of 2b in DMSO-d6

126 MHz 13C-NMR spectra of 2b in DMSO-d6

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500 MHz 1H-NMR spectra of 2c in DMSO-d6

126 MHz 13C-NMR spectra of 2c in DMSO-d6

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500 MHz 1H-NMR spectra of 2d in DMSO-d6

126 MHz 13C-NMR spectra of 2d in DMSO-d6

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500 MHz 1H-NMR spectra of 2e in DMSO-d6

126 MHz 13C-NMR spectra of 2e in DMSO-d6

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500 MHz 1H-NMR spectra of 2f in DMSO-d6

126 MHz 13C-NMR spectra of 2f in DMSO-d6

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500 MHz 1H-NMR spectra of 2g in DMSO-d6

126 MHz 13C-NMR spectra of 2g in DMSO-d6

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500 MHz 1H-NMR spectra of 2h in DMSO-d6

126 MHz 13C-NMR spectra of 2h in DMSO-d6

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500 MHz 1H-NMR spectra of 2i in DMSO-d6

126 MHz 13C-NMR spectra of 2i in DMSO-d6

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500 MHz 1H-NMR spectra of 2j in DMSO-d6

126 MHz 13C-NMR spectra of 2j in DMSO-d6

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500 MHz 1H-NMR spectra of 2k in DMSO-d6

126 MHz 13C-NMR spectra of 2k in DMSO-d6

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500 MHz 1H-NMR spectra of 2l in DMSO-d6

126 MHz 13C-NMR spectra of 2l in DMSO-d6

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500 MHz 1H-NMR spectra of 2m in DMSO-d6

126 MHz 13C-NMR spectra of 2m in DMSO-d6

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500 MHz 1H-NMR spectra of 2n in DMSO-d6

126 MHz 13C-NMR spectra of 2n in DMSO-d6

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500 MHz 1H-NMR spectra of 2o in DMSO-d6

126 MHz 13C-NMR spectra of 2o in DMSO-d6

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500 MHz 1H-NMR spectra of 2p in DMSO-d6

126 MHz 13C-NMR spectra of 2p in DMSO-d6