2004
DOI: 10.1016/j.molcata.2004.05.016
|View full text |Cite
|
Sign up to set email alerts
|

Oxidation of n-heptane with molecular oxygen using heterogeneous catalyst formed by covalently binding [1,2-bis(salicylidene amino)-phenylene] zirconium complex to modified silica gel

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
3
0

Year Published

2006
2006
2020
2020

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 11 publications
(3 citation statements)
references
References 32 publications
0
3
0
Order By: Relevance
“…Such a strategy has been applied [6][7][8][9][10][11][12][13][14][15][16][17][18][19] to the selective partial oxidation of alkanes by transition metal supported catalysts to form oxygencontaining compounds such as alcohols, aldehydes, ketones and carboxylic acids. The alkane oxyfunctionalization constitutes a current challenge to modern chemistry towards the development of highly important and useful reactions for the chemical industry.…”
Section: Introductionmentioning
confidence: 99%
“…Such a strategy has been applied [6][7][8][9][10][11][12][13][14][15][16][17][18][19] to the selective partial oxidation of alkanes by transition metal supported catalysts to form oxygencontaining compounds such as alcohols, aldehydes, ketones and carboxylic acids. The alkane oxyfunctionalization constitutes a current challenge to modern chemistry towards the development of highly important and useful reactions for the chemical industry.…”
Section: Introductionmentioning
confidence: 99%
“…110 Terminally oxidized hydrocarbons are valuable starting materials in the pharmaceutical and chemical industries. 11 However, one of the main challenges in the activation of alkane C–H bonds is the low selectivity in forming the desired products, that is, the preferential activation of sp 2 over sp 3 hybridized C–H bonds. 1214 Furthermore, the chemical inertness of alkanes, together with their high ionization energy, p K a values, and low electron affinity, makes activation of C–H bonds difficult.…”
Section: Introductionmentioning
confidence: 99%
“…1214 Furthermore, the chemical inertness of alkanes, together with their high ionization energy, p K a values, and low electron affinity, makes activation of C–H bonds difficult. 11,13,1517…”
Section: Introductionmentioning
confidence: 99%