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1,4,7,10,25,28,31,34-Octaoxa-[10.10](9,10)-anthracenophane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89317-94-2

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89317-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89317-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,1 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89317-94:
(7*8)+(6*9)+(5*3)+(4*1)+(3*7)+(2*9)+(1*4)=172
172 % 10 = 2
So 89317-94-2 is a valid CAS Registry Number.

89317-94-2Downstream Products

89317-94-2Relevant academic research and scientific papers

Photoresponsive Supramolecular Systems: Synthesis and Photophysical and Photochemical Study of Bis-(9,10-anthracenediyl)coronands AAOnOn

Marquis, Damien,Desvergne, Jean-Pierre,Bouas-Laurent, Henri

, p. 7984 - 7996 (1995)

Monocyclic bis-(9,10-anthracenediyl)coronands denoted AAOnOn (A = (9,10-anthracenediyl, n indicating the number of ethyleneoxy repeating units between two aromatic rings) were designed as photoresponsive systems.Their synthesis is described; their spectroscopic properties were found to be in agreement with the X-ray structures.Special attention was devoted to AAO5O5, which gives coronates with Na(1+) and K(1+).It was observed that one molecule of AAO5O5 displays a positive cooperative effect in binding two sodium cations, in contrast with previous reports on bicyclic coronands.Moreover, in acetonitrile, this effect, clear in the ground state (K11 = 180 M-1, K1,2 = 240 M-1) was found to be stronger in the excited state (K11 = 200 M-1, K1,2 = 500 M-1).With K(1+), AAO5O5 generates a 1:1 complex (K ca. 9 M-1 in methanol).Spectroscopic properties were shown to be triggered by cation concentration, specifically the fluorescence emission which undergoes an important intensity and wavelength redistribution in favor of the excimer: the maximum wavelength is shifted from 530 nm (free ligand) to 570 nm (sodium biscoronate), i.e., Δ ca. 1350 cm-1 and the excimer intensity is multiplied by ca. 3.The photocyclomerization (intramolecular dimerization of the anthracene nucleus) was demonstrated to be regiospecifically directed by Na(1+); in methanol, the free receptor exclusively generates the 9,10:1',4' photoadduct (ΦR ca. 2E-4) whereas the sodium biscoronate leads to the classical 9,10:9',10' photoadduct (ΦR ca. 8E-3).Finally, a transient kinetic analysis versus temperature allowed the determination of the conformational mobility of the free receptor within the nanosecond range; in the singlet excited state it is best described by the sequence M1* -> M2* -> E where M* stands for the locally excited state and E the excimer state species.At room temperature, in methanol, excimer lifetimes were found to be as follows: free ligand, 23 ns; sodium biscoronate, 165 ns; and potassium monocoronate, 215 ns.

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