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Zn(2,3,7,8,12,13,17,18-octakis(3-methoxyphenyl)-5,10,15,20-tetraphenylporphyrin) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

518013-75-7

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518013-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 518013-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,0,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 518013-75:
(8*5)+(7*1)+(6*8)+(5*0)+(4*1)+(3*3)+(2*7)+(1*5)=127
127 % 10 = 7
So 518013-75-7 is a valid CAS Registry Number.

518013-75-7Upstream product

518013-75-7Downstream Products

518013-75-7Relevant academic research and scientific papers

Unusual aryl-porphyrin rotational barriers in peripherally crowded porphyrins

Medforth, Craig J.,Haddad, Raid E.,Muzzi, Cinzia M.,Dooley, Neal R.,Jaquinod, Laurent,Shyr, David C.,Nurco, Daniel J.,Olmstead, Marilyn M.,Smith, Kevin M.,Ma, Jian-Guo,Shelnutt, John A.

, p. 2227 - 2241 (2003)

Previous studies of 5,10,15,20-tetraarylporphyrins have shown that the barrier for meso aryl-porphyrin rotation (ΔG?ROT)) varies as a function of the core substituent M and is lower for a small metal (M = Ni) compared to a large metal (M = Zn) and for a dication (M = 4H2+) versus a free base porphyrin (M = 2H). This has been attributed to changes in the nonplanar distortion of the porphyrin ring and the deformability of the macrocycle caused by the core substituent. In the present work, X-ray crystallography, molecular mechanics (MM) calculations, and variable temperature (VT) 1H NMR spectroscopy are used to examine the relationship between the arylporphyrin rotational barrier and the core substituent M in some novel 2,3,5,7,8,10,12,13,15,17,18,20-dodecaarylporphyrins (DArPs), and specifically in some 5,10,15,20-tetraaryl-2,3,7,8,12,13,17,18-octaphenylporphyrins (TArOPPs), where steric crowding of the peripheral groups always results in a very nonplanar macrocycle. X-ray structures of DArPs indicate differences in the nonplanar conformation of the macrocycle as a function of M, with saddle conformations being observed for M = Zn, 2H or M = 4H2+ and saddle and/or ruffle conformations for M = Ni. VT NMR studies show that the effect of protonation in the TArOPPs is to increase ΔG?ROT, which is the opposite of the effect seen for the TArPs, and MM calculations also predict a strikingly high barrier for the TArOPPs when M = 4H2+. These and other findings suggest that the aryl-porphyrin rotational barriers in the DArPs are closely linked to the deformability of the macrocycle along a nonplanar distortion mode which moves the substituent being rotated out of the porphyrin plane.

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