Unveiling the urease like intrinsic catalytic activities of two dinuclear nickel complexes towards the in situ syntheses of aminocyanopyridinesElectronic supplementary information (ESI) availableSynthetic procedures, instrumentation, and analytical characterization data. Fig. S1–S33 including 1H, 13C NMR, FTIR, ESI-MS, UV-Vis, optical and confocal images. Tables S1–S7, Schemes S1–S3. CCDC 1489559 and 1488864 for complexes 1 and 2, respectively. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d1dt00108f

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Title: Unveiling the urease like intrinsic catalytic activities of two dinuclear nickel complexes towards the in situ syntheses of aminocyanopyridinesElectronic supplementary information (ESI) availableSynthetic procedures, instrumentation, and analytical characterization data. Fig. S1–S33 including 1H, 13C NMR, FTIR, ESI-MS, UV-Vis, optical and confocal images. Tables S1–S7, Schemes S1–S3. CCDC 1489559 and 1488864 for complexes 1 and 2, respectively. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d1dt00108f
Authors: Kundu, Bidyut Kumar, Biswas, Soumen, Mondal, Abhijit, Mazumdar, Shyamalava, Mobin, Shaikh M., Mukhopadhyay, Suman
Source: Dalton transactions. 50(14):4848-4858
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  Data: Unveiling the urease like intrinsic catalytic activities of two dinuclear nickel complexes towards the in situ syntheses of aminocyanopyridinesElectronic supplementary information (ESI) availableSynthetic procedures, instrumentation, and analytical characterization data. Fig. S1–S33 including 1H, 13C NMR, FTIR, ESI-MS, UV-Vis, optical and confocal images. Tables S1–S7, Schemes S1–S3. CCDC 1489559 and 1488864 for complexes 1 and 2, respectively. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d1dt00108f
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      – TitleFull: Unveiling the urease like intrinsic catalytic activities of two dinuclear nickel complexes towards the in situ syntheses of aminocyanopyridinesElectronic supplementary information (ESI) availableSynthetic procedures, instrumentation, and analytical characterization data. Fig. S1–S33 including 1H, 13C NMR, FTIR, ESI-MS, UV-Vis, optical and confocal images. Tables S1–S7, Schemes S1–S3. CCDC 1489559 and 1488864 for complexes 1 and 2, respectively. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d1dt00108f
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