Electronic effects of the substituent on the dioxygen-activating abilities of substituted iron tetraphenylporphyrins: a theoretical study-Reference-Cited by-同舟云学术

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Electronic effects of the substituent on the dioxygen-activating abilities of substituted iron tetraphenylporphyrins: a theoretical study

Published:2015-03-19 Issue:4 Volume:21 Page:
ISSN:1610-2940
Container-title:Journal of Molecular Modeling
language:en
Short-container-title:J Mol Model

Author:

Fu Haiyan,Cao Meijuan,She Yuanbin,Sun Zhicheng,Yu Yanmin

Publisher

Springer Science and Business Media LLC

Subject

Computational Theory and Mathematics,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Catalysis

Link

http://link.springer.com/content/pdf/10.1007/s00894-015-2619-z.pdf

Reference48 articles.

1. Tse C, Chow TW, Guo Z, Lee HK, Huang J, Che C (2014) Nonheme iron mediated oxidation of light alkanes with oxone: characterization of reactive oxoiron(IV) ligand cation radical intermediates by spectroscopic studies and DFT calculations. Angew Chem Int Ed 126:817–822

2. Yang X, Xie M, Zou C, He Y, Chen BO, Keeffe M, Wu C (2012) Porous metalloporphyrinic frameworks constructed from metal 5,10,15,20-tetrakis(3,5-biscarboxylphenyl) porphyrin for highly efficient and selective catalytic oxidation of alkylbenzenes. J Am Chem Soc 134:10638–10645

3. Lee J, Farha OK, Roberts J, Scheidt KA, Nguyen ST, Hupp JT (2009) Metal–organic framework materials as catalysts. Chem Soc Rev 38:1450–1459

4. Kim S, Hyun MY, Hong J, Huh S, Kim C, Lee SJ (2012) Controlled growth of narrowly dispersed nanosize hexagonal MOF rods from Mn(III)-porphyrin and in (NO3)3 and their application in olefin oxidation. Chem Commun 48:5512–5514

5. Hajimohammadi M, Safari N, Mofakham H, Deyhimi F (2011) Highly selective, economical and efficient oxidation of alcohols to aldehydes and ketones by air and sunlight or visible light in the presence of porphyrin sensitizers. Green Chem 13:991–997

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