Microwave-assisted functionalization of the Aurivillius phase Bi2SrTa2O9: diol grafting and amine insertion vs. alcohol grafting. Issue 35 (1st August 2018)
- Record Type:
- Journal Article
- Title:
- Microwave-assisted functionalization of the Aurivillius phase Bi2SrTa2O9: diol grafting and amine insertion vs. alcohol grafting. Issue 35 (1st August 2018)
- Main Title:
- Microwave-assisted functionalization of the Aurivillius phase Bi2SrTa2O9: diol grafting and amine insertion vs. alcohol grafting
- Authors:
- Wang, Yanhui
Nikolopoulou, Maria
Delahaye, Emilie
Leuvrey, Cédric
Leroux, Fabrice
Rabu, Pierre
Rogez, Guillaume - Abstract:
- Abstract : The microwave-assisted functionalization of an Aurivillius phase is investigated towards various molecules – alcohols, diols and amino-alcohols – and the preferential reactivity of the various moieties is studied as a function of the reaction conditions. Abstract : Microwave-assisted functionalization of the layered Aurivillius phase Bi2 SrTa2 O9 by alcohols is thoroughly investigated. The grafting of linear aliphatic and bulky alcohols is studied as a function of the starting material, underlining the importance of the prefunctionalization of the layered perovskite, for instance by butylamine. In addition, the functionalization by α, ω-alkanediols is explored. α, ω-alkanediols bearing long alkyl chains ( n C > 3) adopt an unprecedented pillaring arrangement, whereas 1, 3-propanediol and ethyleneglycol adopt a bilayer arrangement, only one out of the two hydroxyl groups being coordinated. Finally, the reactivities of alcohols and amines towards insertion are compared: the preferential reactivity of the two functional groups appears to be strongly dependent of the reaction conditions, and especially of the water content. This study is further extended to the case of amino-alcohol insertion. In this case, the amine group is preferentially bound, but it is possible to control the grafting of the alcohol moiety, thus going from a bilayer arrangement to a pillaring one. This work is of particular importance to be able to functionalize easily and rapidly layered oxidesAbstract : The microwave-assisted functionalization of an Aurivillius phase is investigated towards various molecules – alcohols, diols and amino-alcohols – and the preferential reactivity of the various moieties is studied as a function of the reaction conditions. Abstract : Microwave-assisted functionalization of the layered Aurivillius phase Bi2 SrTa2 O9 by alcohols is thoroughly investigated. The grafting of linear aliphatic and bulky alcohols is studied as a function of the starting material, underlining the importance of the prefunctionalization of the layered perovskite, for instance by butylamine. In addition, the functionalization by α, ω-alkanediols is explored. α, ω-alkanediols bearing long alkyl chains ( n C > 3) adopt an unprecedented pillaring arrangement, whereas 1, 3-propanediol and ethyleneglycol adopt a bilayer arrangement, only one out of the two hydroxyl groups being coordinated. Finally, the reactivities of alcohols and amines towards insertion are compared: the preferential reactivity of the two functional groups appears to be strongly dependent of the reaction conditions, and especially of the water content. This study is further extended to the case of amino-alcohol insertion. In this case, the amine group is preferentially bound, but it is possible to control the grafting of the alcohol moiety, thus going from a bilayer arrangement to a pillaring one. This work is of particular importance to be able to functionalize easily and rapidly layered oxides with elaborated molecules, bearing several different potentially reactive groups. … (more)
- Is Part Of:
- Chemical science. Volume 9:Issue 35(2018)
- Journal:
- Chemical science
- Issue:
- Volume 9:Issue 35(2018)
- Issue Display:
- Volume 9, Issue 35 (2018)
- Year:
- 2018
- Volume:
- 9
- Issue:
- 35
- Issue Sort Value:
- 2018-0009-0035-0000
- Page Start:
- 7104
- Page End:
- 7114
- Publication Date:
- 2018-08-01
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8sc01754a ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7684.xml