unveiling the effects of generated arene anion …supporting information unveiling the effects of...
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Supporting Information
Unveiling the effects of in situ generated arene anion radical and imine
radical on catecholase like activity: A DFT supported experimental
investigation
Sanchari Dasgupta,a Jaydeep Adhikary,a Sanjib Giri, a Antonio Bauza, bAntonio Frontera,
b and Debasis Das*,a
aDepartment of Chemistry, University of Calcutta, 92, A. P. C. Road, Kolkata – 700009,
India.
bDepartament de Química, Universitat de les Illes Balears, Crta. de Valldemossa km 7.5, 07122, Palma (Baleares), Spain
Fig. S1 FTIR spectrum of complex 1.
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Electronic Supplementary Material (ESI) for Dalton Transactions.This journal is © The Royal Society of Chemistry 2017
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Fig. S2 FTIR spectrum of complex 2
(a)
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(b)
Fig. S3 UV-Vis spectra of complexes.
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Fig.S4 ESI-MS spectrum of complex 1.
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Fig. S5 ESI-MS spectrum of complex 2.
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(a)
(b) Fig. S6 Cyclic voltammetry of (a) complex 1 and (b) complex 2
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Fig. S7 Solid UV-Vis spectra of complexes.
Fig. S8 Detection of H2O2 formation during oxidation of 3,5-DTBC observed spectrophotometrically
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(a)
(b)
Fig. S9 (a) Dependence of rate of reaction on substrate concentration for Complex 1 and 2(100 μM) and (b) Lineweaver−Burk plots for Complex 1 and 2 at 25°C in Acetonitrile (100
μM) for oxidation of Catechol
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Fig. S10 ESI-MS spectra of reaction mixture of complex 1 and 3,5-DTBC recorded at different time interval.
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Fig. S11 ESI-MS spectra of reaction mixture of complex 2 and 3,5-DTBC recorded at different time interval.
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(a)
(b)
Fig. S12 EPR spectra of (a) complex 1 and (b) complex 2 in acetonitrile medium
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Table S1 Selected parameters for vertical excitation (UV-vis absorptions) of 1 and 2. Electronic excitation energies (eV), oscillator strengths (f), configurations of the two lowest lying excited states of 1 and 2; calculation of the S0–Sn energy gaps based on optimized ground-state geometries (UV-vis absorption) (CH3CN used as solvent)
Process Electronic
transitions Composition Excitation energy
(λ) Oscillator strength
(f)
λexp (nm)
Complex 1 Absorption S0 → S1 HOMO →
LUMO (100%) 1.4238 eV (871
nm) 0.0002 950-980
Absorption S0 → S2 HOMO → LUMO+1
(96%)
1.8920 eV (655 nm)
0.0045 610-690
Complex 2 Absorption S0 → S1 HOMO →
LUMO (100%) 1.2853 eV (965
nm) 0.0029 950-980
Absorption S0 → S2 HOMO–1 → LUMO (36%) HOMO–2 → LUMO (13%) HOMO–3 → LUMO (51%)
2.0339 eV (610 nm)
0.0104
610-690
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Fig. S13Frontier molecular orbitals involved in the two lowest UV-vis absorption bands of complex 1 in acetonitrile.
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Fig. S14 Frontier molecular orbitals involved in the two lowest UV-vis absorption bands of complex 2 in acetonitrile.
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