Investigation of the interactions involved in the formation of nanotubes from organogelators

Investigations into the formation of nanosized structures, particularly nanotubes, by a diamide ester compound are reported. Two aspects are concurrently examined: the role of the solvent and the role of the alkyl chain. The former is addressed by using a benzene derivative (o-xylene) and a totally...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 29(2013), 52 vom: 31. Dez., Seite 16127-34
1. Verfasser: Khan, Ahmad Nawaz (VerfasserIn)
Weitere Verfasser: Nguyen, Thi-Thanh-Tam, Dobircau, Larisa, Schmutz, Marc, Mesini, Philippe J, Guenet, Jean-Michel
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
LEADER 01000caa a22002652 4500
001 NLM233498680
003 DE-627
005 20250216103213.0
007 cr uuu---uuuuu
008 231224s2013 xx |||||o 00| ||eng c
024 7 |a 10.1021/la404002k  |2 doi 
028 5 2 |a pubmed25n0778.xml 
035 |a (DE-627)NLM233498680 
035 |a (NLM)24321040 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Khan, Ahmad Nawaz  |e verfasserin  |4 aut 
245 1 0 |a Investigation of the interactions involved in the formation of nanotubes from organogelators 
264 1 |c 2013 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 27.08.2014 
500 |a Date Revised 31.12.2013 
500 |a published: Print-Electronic 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a Investigations into the formation of nanosized structures, particularly nanotubes, by a diamide ester compound are reported. Two aspects are concurrently examined: the role of the solvent and the role of the alkyl chain. The former is addressed by using a benzene derivative (o-xylene) and a totally saturated double ring (trans-decahydronaphthalene) whereas the latter is achieved by replacing the hydrogenous alkyl chain with its fluorinated counterpart while keeping the overall architecture the same. The thermodynamic behavior by differential scanning calorimetry, the morphology by transmission electron microscopy, and the structure by X-ray scattering and small-angle neutron scattering are studied. Despite the identical architecture, the fluorinated molecule does not produce any nanotubes, unlike its totally hydrogenous counterpart. Also, o-xylene prevents the hydrogenous molecule from forming nanotubes, while nanotapes are produced instead. Conversely, the fluorinated molecule produces regularly twisted protostructures in either solvent. Neutron scattering experiments show that the fluorinated alky chain is located within the core of this structure. This suggests that the prerequisite for forming nanotubes relies on the necessity of the alkyl group to point outward 
650 4 |a Journal Article 
700 1 |a Nguyen, Thi-Thanh-Tam  |e verfasserin  |4 aut 
700 1 |a Dobircau, Larisa  |e verfasserin  |4 aut 
700 1 |a Schmutz, Marc  |e verfasserin  |4 aut 
700 1 |a Mesini, Philippe J  |e verfasserin  |4 aut 
700 1 |a Guenet, Jean-Michel  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1985  |g 29(2013), 52 vom: 31. Dez., Seite 16127-34  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:29  |g year:2013  |g number:52  |g day:31  |g month:12  |g pages:16127-34 
856 4 0 |u http://dx.doi.org/10.1021/la404002k  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |d 29  |j 2013  |e 52  |b 31  |c 12  |h 16127-34