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[Cu(cyclo-6,6'-[1,9-(2,5,8-trithianonane)]-2,2'-bipyridine)]1+ is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

936742-15-3

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936742-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936742-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,7,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 936742-15:
(8*9)+(7*3)+(6*6)+(5*7)+(4*4)+(3*2)+(2*1)+(1*5)=193
193 % 10 = 3
So 936742-15-3 is a valid CAS Registry Number.

936742-15-3Downstream Products

936742-15-3Relevant articles and documents

A definitive example of a geometric entatic state effect: Electron-transfer kinetics for a copper(ll/l) complex involving a quinquedentate macrocyclic trithiaether - Bipyridine ligand

Chaka, Gezahegn,Sonnenberg, Jason L.,Schlegel, H. Bernhard,Heeg, Mary Jane,Jaeger, Gregory,Nelson, Timothy J.,Ochrymowycz,Rorabacher

, p. 5217 - 5227 (2007)

The quinquedentate macrocyclic ligand cyclo-6,6′-[1,9-(2,5,8- trithianonane)]-2,2′-bipyridine ([15]aneS3bpy = L), containing two pyridyl nitrogens and three thiaether sulfurs as donor atoms, has been synthesized and complexed with copper. The CuII/I redox potential, the stabilities of the oxidized and reduced complex, and the oxidation and reduction electron-transfer kinetics of the complex reacting with a series of six counter reagents have been studied in acetonitrile at 25°C, μ = 0.10 M (NaCIO4). The Marcus cross relationship has been applied to the rate constants obtained for the reactions with each of the six counter reagents to permit the evaluation of the electron self-exchange rate constant, k 11. The latter value has also been determined independently from NMR line-broadening experiments. The cumulative data are consistent with a value of k11 = 1 × 105 M-1 s1, ranking this among the fastest-reacting CuII/I systems, on a par with the blue copper proteins known as cupredoxins. The resolved crystal structures show that the geometry of the CuIIL and CuIL complexes are nearly identical, both exhibiting a five-coordinate square pyramidal geometry with the central sulfur donor atom occupying the apical site. The most notable geometric difference is a puckering of an ethylene bridge between two sulfur donor atoms in the CuIL complex. Theoretical calculations suggest that the reorganizational energy is relatively small, with the transition-state geometry more closely approximating the geometry of the CuIIL ground state. The combination of a nearly constant geometry and a large self-exchange rate constant implies that this CuII/I redox system represents a true geometric entatic state.

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