Regioselectivity of Complexations of Substituted Phenyl Benzoates and Phenyl Phenylacetates with Cr(CO)6

1994 ◽  
Vol 59 (9) ◽  
pp. 2095-2102
Author(s):  
Pavol Hrnčiar ◽  
Peter Černák ◽  
Vladimír Gajda ◽  
Štefan Toma

Selectivity of complexation of substituted phenyl benzoates is very low. In most cases, comparable yields of both regioisomeric complexes are isolated. Exception is 4-chlorophenyl ester, where benzoic acid moiety is complexed nearly exclusively. Very high regioselectivity of complexation was observed with substituted phenyl phenylacetates. The substituent of substituted phenols has not any effect on the complexation, and only phenylacetic acid moiety is complexed. This observation supports the recently proposed mechanism of the catalytic activity of the esters at arene complexation.

2021 ◽  
pp. 115737
Author(s):  
Dimitris Matiadis ◽  
Katarzyna E. Nowak ◽  
Eleni Alexandratou ◽  
Antonios Hatzidimitriou ◽  
Marina Sagnou ◽  
...  

1933 ◽  
Vol 8 (5) ◽  
pp. 447-449 ◽  
Author(s):  
Steward Basterfield ◽  
James W. Tomecko

The ionization constants of p-nitrophenylacetic and phenylmalonic acids have been determined from conductivity data. The value of K for p-nitrophenylacetic acid at 25 °C. is 1.04 × 10−4, about twice that of phenylacetic acid. The nitro group in the nucleus has not as powerful an effect on the ionization when the COOH group is in the side chain as it has when both nitro group and COOH are in the nucleus. K for p-nitrobenzoic acid is six times as great as K for benzoic acid. K for phenylmalonic acid is 2. 77 × 10−3 as compared with 1.6 × 10−3 for malonic acid.


2012 ◽  
Vol 583 ◽  
pp. 285-288
Author(s):  
Dong Mei Zhao ◽  
Xue Peng Liu

By orthogonal design method, Catalytic activity of /ZrO2 solid superacid is studied, and the influence of catalyst characteristic and structure by manufacturing equipment is issued. It is concluded that the best prepared conditions of the superacid catalyst /ZrO2 for the synthesis of Octyl-Polyglycoside are followed:(1) PH=9.5; (2) calcined temperature at 500; (3) M(H2SO4)=0.5mol/L. Using this kind of catalyst the conversion of glueoside may reach as high as 96% in the synthesis of OCtyl-Polyglycoside and the selectivity is very high for the synthesis of Octyl-Polyglycoside. By introducing other metal oxide, the catalytic activity of complex solid superacid is studied.


RSC Advances ◽  
2016 ◽  
Vol 6 (29) ◽  
pp. 24097-24102 ◽  
Author(s):  
Betül Çelik ◽  
Yunus Yıldız ◽  
Hakan Sert ◽  
Esma Erken ◽  
Yagmur Koşkun ◽  
...  

Monodispersed PdCo@PVP NPs showed record catalytic activity, giving the best catalytic performance yet with a very high turnover frequency.


2004 ◽  
Vol 20 (2) ◽  
pp. 273-278 ◽  
Author(s):  
Jun NAKANISHI ◽  
Mizuo MAEDA ◽  
Yoshio UMEZAWA

2011 ◽  
Vol 81 (9) ◽  
pp. 1839-1844 ◽  
Author(s):  
L. Shteinberg ◽  
V. V. Marshalova ◽  
V. M. Dibrova ◽  
S. M. Shein

2014 ◽  
Vol 18 (07) ◽  
pp. 604-613 ◽  
Author(s):  
Anna S. Makarova ◽  
Evgeny V. Kudrik ◽  
Sergei V. Makarov ◽  
Oskar I. Koifman

A study of catalytic activity of μ-nitrido- and μ-oxo-dimeric iron tetrasulfophthalocyanines in the oxidation of Orange II by tert-butylhydroperoxide in aqueous solutions has been performed. It is shown that though in one catalytic cycle activity of μ-oxo-dimer is higher, stability of this complex in oxidative conditions is poor. μ-nitrido-dimer combines relatively good catalytic activity with very high stability in the presence of tert-butylhydroperoxide. The mechanisms of oxidative decomposition of dimers and catalytic oxidation of Orange II have been proposed on the base of kinetic results. The products of catalytic processes are shown to be bio-degradable non-toxic small organic compounds.


2016 ◽  
Vol 43 (5) ◽  
pp. 2921-2929 ◽  
Author(s):  
Nuonuo Zhang ◽  
Jiaqi Chen ◽  
Kai Cheng ◽  
Yujiao Li ◽  
Long Wang ◽  
...  

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