Cyclic voltammogram CH3CN solution

Fig. 17.4 Cyclic Voltammogram of 5 niM solution of [RelCOljClJjtbpq on 1 mm Pt wire, in SEC cell (0.2 M TBAPF/CH3CN)...

For example, the complexes [Mn (N)(CN)4] and [Mn (L)3] (L = benzohydroxamic acid) in CH3CN solutions show irreversible anodic responses in their cyclic voltammograms suggesting Mn and Mn complexes are formed. ... 

Figure 2. Cyclic voltammograms (0.1 V s"1) at a Pt disk electrode in 2 1 CH3CN-benzene (v/v) containing (a) 0.1 M TBABFi, and 20 mM (TBA)2S208, (b) solution (a) with 1.0 mM RUB, (c) relative ECL intensity vs. potential for solution (b).

VOV(salen)][BF4]2 after controlled potential oxidation that consumed one electron per dinuclear molecule. Pt disk (o = 4 mm), 500 rpm, anaerobic anhydrous CH3CN, TBABF4 (0.1 mol/1) (b) cyclic voltammogram for the solution from (a). 

Figure 1. Cyclic voltammograms of a 1.0 x 10 M solution of [Pd(IPNetpE)(CH3CN)](BF4)2 in DMF under Nz (left-hand graph, open circles) and in the presence of 0.18 CO2 (left-hand graph, solid line). The right-hand graph shows cyclic voltammograms of the same solution after adding acid (0.04 M HBF4) under Nz (open circles) and CO2 (solid line).

Fig. 2.2 Normalized UV-vi s absorption spectra of a IIDDT and b IIDT in CHCI3 (1 x 10 M), in thin film, and in annealed film (at 150 °C for 20 min), c Cyclic voltammogram of IIDDT and IIDT in thin film drop-casting on a glassy carbon and tested in BU4NPF6/CH3CN solution (scan rate 50 mV s ). The oxidative currents are almost an order of magnitude higher, d Calculated molecular orbitals of the IIDDT trimer (B3LYP/6-31G (d))...

Fig. 2.13 Cyclic voltammogram of polymers in thin film drop-casted on a glassy carbon electrode and tested in n-Bu4NPF6/CH3CN solution (scan rate ...

Fig. 6 Cyclic voltammograms of benzanthrone (a), thiophene (f) and the monomer mixtures with benzanthrone/thiophene = 5 2 (b), 1 1 (c), 1 3 (d), and 1 5 (e), respectively, in BFEE/CH3CN (9 1 vol) solutions, v = 100 mV s . Reproduced with permission from ref. 101, Copyright 2010 Springer-Verlag.

Fig. 7 Emission spectra of (a) DHQT, (b) PDHQT, P(DHQT-co-DNBP) prepared with (c) 1 1 and (d) 1 5 feed ratios, in NMP solution (excitation at 375 nm). Inset photoluminescence of (a) DHQT, (b) PDHQT, P(DHQT-co-DNBP) prepared with (c) 1 land (d) l 5feed ratios, in NMP solution, when exposed to UV light (A) and cyclic voltammograms of PDHQT(a) and P(DHQT-co-DNBP) films deposited onto ITQ/glass in (b) 1 1, (c) 1 3, (d) 1 5 and (e) 1 8 feed ratios in 0.1 mol (C4H9)4NBp4/CH3CN (B), v = 20 mVs . Reproduced with permission from ref. 105, Copyright 2014 Elsevier.

Figure 9. Cyclic voltammograms of 12 (top) and 14 (below) (1 mM) with 0-4 mM HOTs in 0.1 M n-Bu4NPF /CH3CN solution at a potential scan rate of 100 mVs. ...

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