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19137-07-6

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19137-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19137-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,3 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19137-07:
(7*1)+(6*9)+(5*1)+(4*3)+(3*7)+(2*0)+(1*7)=106
106 % 10 = 6
So 19137-07-6 is a valid CAS Registry Number.

19137-07-6Downstream Products

19137-07-6Relevant articles and documents

Spin-Doctoring Cobalt Redox Shuttles for Dye-Sensitized Solar Cells

Baillargeon, Josh,Xie, Yuling,Raithel, Austin L.,Ghaffari, Behnaz,Staples, Richard J.,Hamann, Thomas W.

, p. 11633 - 11645 (2018)

A new low-spin (LS) cobalt(II) outer-sphere redox shuttle (OSRS) [Co(PY5Me2)(CN)]+, where PY5Me2 represents the pentadentate ligand 2,6-bis(1,1-bis(2-pyridyl)ethyl)pyridine, has been synthesized and characterized for its potential application in dye-sensitized solar cells (DSSCs). Introduction of the strong field CN- ligand into the open axial coordination site forced the cobalt(II) complex, [Co(PY5Me2)(CN)]+, to become LS based upon the complex's magnetic susceptibility (1.91 ± 0.02 μB), determined by the Evans method. Interestingly, dimerization and subsequent cobalt hexacyanide cluster formation of the [Co(PY5Me2)(CN)]+ monomer was observed upon long-term solvent exposure or addition of a supporting electrolyte for electrochemical characterization. Although long-term stability of the [Co(PY5Me2)(CN)]+ complex made it difficult to fabricate liquid electrolytes for DSSC applications, short-term stability in neat solvent afforded the opportunity to isolate the self-exchange kinetics of [Co(PY5Me2)(CN)]2+/+ via stopped-flow spectroscopy. Use of Marcus theory provided a smaller than expected self-exchange rate constant of 20 ± 5.5 M-1 s-1 for [Co(PY5Me2)(CN)]2+/+, which we attribute to a Jahn-Teller effect observed from the collected monomer crystallographic data. When compared side-by-side to cobalt tris(2,2′-bipyridine), [Co(bpy)3]3+, DSSCs employing [Co(PY5Me2)(CN)]2+ are expected to achieve superior charge collection, which result from a smaller rate constant, ket, for recombination based upon simple dark J-E measurements of the two redox shuttles. Given the negative redox potential (0.254 V vs NHE) of [Co(PY5Me2)(CN)]2+/+ and the slow recombination kinetics, [Co(PY5Me2)(CN)]2+/+ becomes an attractive OSRS to regenerate near IR absorbing sensitizers in solid-state DSSC devices.

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