In situ formation of AuNPs using fatty N-acylamino hydrazide organogelators as templates. (28th November 2018)
- Record Type:
- Journal Article
- Title:
- In situ formation of AuNPs using fatty N-acylamino hydrazide organogelators as templates. (28th November 2018)
- Main Title:
- In situ formation of AuNPs using fatty N-acylamino hydrazide organogelators as templates
- Authors:
- Ongaratto, Renata
Conte, Naiane
Montes D'Oca, Caroline R.
Brinkerhoff, Rafael C.
Ruas, Caroline Pires
Gelesky, Marcos Alexandre
Montes D'Oca, Marcelo G. - Abstract:
- Abstract : This work reports, for the first time, the synthesis of new fatty N -acylamino hydrazides and demonstrates the activity of these compounds as low-molecular-weight organic gelators and templates for preparation of gold nanoparticles (AuNPs). Abstract : This work reports, for the first time, the synthesis of new fatty N -acylamino hydrazides and demonstrates the activity of these compounds as low-molecular-weight organic gelators and templates for preparation of gold nanoparticles (AuNPs). Initially, we evaluated the gelation properties of fatty N -acylamino hydrazides in various nonpolar and polar solvents ( n -hexane, toluene, benzene, cyclohexane, and ethanol). Fatty N -acylamino hydrazide derived of the glycine and stearic acid (C18:0) did not form gels in any of the tested solvents. All other hydrazides did form gels in at least two of the organic solvents tested. The morphology of each gel was observed via scanning electron microscopy. The organogels derived from alanine, valine, and phenylalanine had translucid properties, while the serine organogels were opaque. Afterwards, the synthesis of AuNPs in the presence of the organogelator using microwave irradiation was realized. Organogelator agents reduced HAuCl4 showing plasmon band peaks between 530 and 543 nm. In addition, the method does not require a reducing agent, which is typically a potential source of contamination and toxicity. Therefore, this work confirms the importance of the hydrazide group of theAbstract : This work reports, for the first time, the synthesis of new fatty N -acylamino hydrazides and demonstrates the activity of these compounds as low-molecular-weight organic gelators and templates for preparation of gold nanoparticles (AuNPs). Abstract : This work reports, for the first time, the synthesis of new fatty N -acylamino hydrazides and demonstrates the activity of these compounds as low-molecular-weight organic gelators and templates for preparation of gold nanoparticles (AuNPs). Initially, we evaluated the gelation properties of fatty N -acylamino hydrazides in various nonpolar and polar solvents ( n -hexane, toluene, benzene, cyclohexane, and ethanol). Fatty N -acylamino hydrazide derived of the glycine and stearic acid (C18:0) did not form gels in any of the tested solvents. All other hydrazides did form gels in at least two of the organic solvents tested. The morphology of each gel was observed via scanning electron microscopy. The organogels derived from alanine, valine, and phenylalanine had translucid properties, while the serine organogels were opaque. Afterwards, the synthesis of AuNPs in the presence of the organogelator using microwave irradiation was realized. Organogelator agents reduced HAuCl4 showing plasmon band peaks between 530 and 543 nm. In addition, the method does not require a reducing agent, which is typically a potential source of contamination and toxicity. Therefore, this work confirms the importance of the hydrazide group of the new fatty N -acylamino hydrazides in gel formation and as organogelator agents for preparation of AuNPs. … (more)
- Is Part Of:
- New journal of chemistry. Volume 43:Number 1(2019)
- Journal:
- New journal of chemistry
- Issue:
- Volume 43:Number 1(2019)
- Issue Display:
- Volume 43, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 43
- Issue:
- 1
- Issue Sort Value:
- 2019-0043-0001-0000
- Page Start:
- 295
- Page End:
- 303
- Publication Date:
- 2018-11-28
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c8nj04127j ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9291.xml