alpha-Pinene oxide isomerization: role of zeolite structure and acidity in the selective synthesis of campholenic aldehyde

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F18%3A00490675" target="_blank" >RIV/61388955:_____/18:00490675 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1039/c8cy00371h" target="_blank" >http://dx.doi.org/10.1039/c8cy00371h</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c8cy00371h" target="_blank" >10.1039/c8cy00371h</a>

Jazyk výsledku

angličtina

Název v původním jazyce

alpha-Pinene oxide isomerization: role of zeolite structure and acidity in the selective synthesis of campholenic aldehyde

Popis výsledku v původním jazyce

MWW-type zeolites with different textural properties, namely, MCM-22, MCM-36, MCM-56, and MCM-49, were synthesized and tested in the selective preparation of campholenic aldehyde by isomerization ofpinene oxide. Commercial zeolites USY, Beta, and ZSM-5 were compared. The physico-chemical properties of the studied zeolites were correlated with their catalytic performance in the isomerization ofpinene oxide carried out either in toluene as a solvent at 70 degrees C or in N,N-dimethylacetamide at 140 degrees C.Pinene oxide isomerizes easily in the presence of acids and therefore, high conversions were achieved over commercial as well as synthesized MWW catalysts. Higher selectivities to campholenic aldehyde were achieved over MWW catalysts in basic N,N-dimethylacetamide while non-basic toluene enhanced the formation of the desired aldehyde over all the commercial zeolites. The highest selectivity to the desired aldehyde was achieved over MCM-22 in the reaction performed in N,N-dimethylacetamide at 140 degrees C, being 83% at total conversion ofpinene oxide. This is the best result achieved rivaling homogenous acids (ZnBr2) and metal-organic frameworks.

Název v anglickém jazyce

alpha-Pinene oxide isomerization: role of zeolite structure and acidity in the selective synthesis of campholenic aldehyde

Popis výsledku anglicky

MWW-type zeolites with different textural properties, namely, MCM-22, MCM-36, MCM-56, and MCM-49, were synthesized and tested in the selective preparation of campholenic aldehyde by isomerization ofpinene oxide. Commercial zeolites USY, Beta, and ZSM-5 were compared. The physico-chemical properties of the studied zeolites were correlated with their catalytic performance in the isomerization ofpinene oxide carried out either in toluene as a solvent at 70 degrees C or in N,N-dimethylacetamide at 140 degrees C.Pinene oxide isomerizes easily in the presence of acids and therefore, high conversions were achieved over commercial as well as synthesized MWW catalysts. Higher selectivities to campholenic aldehyde were achieved over MWW catalysts in basic N,N-dimethylacetamide while non-basic toluene enhanced the formation of the desired aldehyde over all the commercial zeolites. The highest selectivity to the desired aldehyde was achieved over MCM-22 in the reaction performed in N,N-dimethylacetamide at 140 degrees C, being 83% at total conversion ofpinene oxide. This is the best result achieved rivaling homogenous acids (ZnBr2) and metal-organic frameworks.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

<a href="/cs/project/GA17-01440S" target="_blank" >GA17-01440S: Příprava pokročilých katalyzátoru ze stavebnicových jednotek</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Catalysis Science &Technology

ISSN

2044-4753

e-ISSN

—

Svazek periodika

8

Číslo periodika v rámci svazku

9

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

14

Strana od-do

2488-2501

Kód UT WoS článku

000433163900025

EID výsledku v databázi Scopus

2-s2.0-85046945180