2011
DOI: 10.1016/j.clay.2010.09.016
|View full text |Cite
|
Sign up to set email alerts
|

Organic synthesis using clay and clay-supported catalysts

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

4
114
0
3

Year Published

2013
2013
2023
2023

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 216 publications
(121 citation statements)
references
References 97 publications
4
114
0
3
Order By: Relevance
“…Since the catalytic affect of the clay can be attributed to the Lewis acid activity of its metallic centers (Scheme 2a), the good reactivity of the methoxy derivatives can be explained by accepting that coordination of the oxygen atom in the OMe group with cationic centers in the clay attenuates its electron-releasing effect (Scheme 2b) [40]. Another special case was that of nitrobenzaldehyde derivatives which, again unexpectedly, gave relatively low yields (entries 7,8,9,13,18,22,25,[30][31][32][33][34][35]. In this case, we propose that the lower reactivity is due to an increased activation energy associated to stabilizing interactions of the aldehyde with the clay by coordinating two of the cationic centers (Scheme 2c).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Since the catalytic affect of the clay can be attributed to the Lewis acid activity of its metallic centers (Scheme 2a), the good reactivity of the methoxy derivatives can be explained by accepting that coordination of the oxygen atom in the OMe group with cationic centers in the clay attenuates its electron-releasing effect (Scheme 2b) [40]. Another special case was that of nitrobenzaldehyde derivatives which, again unexpectedly, gave relatively low yields (entries 7,8,9,13,18,22,25,[30][31][32][33][34][35]. In this case, we propose that the lower reactivity is due to an increased activation energy associated to stabilizing interactions of the aldehyde with the clay by coordinating two of the cationic centers (Scheme 2c).…”
Section: Resultsmentioning
confidence: 99%
“…In particular, there is much interest in the use of clays as solid acid catalysts because of their desirable properties such as environmental compatibility, non-corrosive and non-toxic nature, low cost and, furthermore, because they often allow very simple isolation procedures. To summarize, heterogeneous catalysis is crucial to chemical technology, and clays in particular are finding increasing applications as catalysts [31][32][33][34].…”
Section: Introductionmentioning
confidence: 99%
“…This hypothesis is consistent with the documented ability of clay minerals to catalyze condensation and polymerization reactions from a variety of substrates. [35][36][37] This effect is of particular importance, since the low-molecular weight degradation products have been shown to have a mutagenic potential 38 .At pyrolysis temperatures of 450 °C -550 °C, the 13 C NMR signal is very similar in all the materials being centered at ~ 130 pm as see in Figure 2 (g-l). The primary species produced at these temperatures have an aromatic carbon structure, in addition to some phenolic and carboxylic species observed at ~150-160 ppm and 165-180 ppm, respectively.…”
Section: Infiltrationmentioning
confidence: 93%
“…Montmorillonite K10 (MMT K10), the major clay mineral commercially available has been used as a heterogeneous catalyst for many applications [5], [6]. There are considerable methods which can be used to modify MMT to improve its catalytic properties, such of these methods include cation exchanged.…”
Section: Introductionmentioning
confidence: 99%