Diacetylenes with Ionic‐Liquid‐Like Substituents: Associating a Polymerizing Cation with a Polymerizing Anion in a Single Precursor for the Synthesis of N‐Doped Carbon Materials. Issue 5 (23rd December 2015)
- Record Type:
- Journal Article
- Title:
- Diacetylenes with Ionic‐Liquid‐Like Substituents: Associating a Polymerizing Cation with a Polymerizing Anion in a Single Precursor for the Synthesis of N‐Doped Carbon Materials. Issue 5 (23rd December 2015)
- Main Title:
- Diacetylenes with Ionic‐Liquid‐Like Substituents: Associating a Polymerizing Cation with a Polymerizing Anion in a Single Precursor for the Synthesis of N‐Doped Carbon Materials
- Authors:
- Fahsi, Karim
Dumail, Xavier
Dutremez, Sylvain G.
van der Lee, Arie
Vioux, André
Viau , Lydie - Abstract:
- Abstract: Imidazolium‐ and benzimidazolium‐substituted diacetylenes with bromide or nitrogen‐rich dicyanamide and tricyanomethanide anions were synthesized and used as precursors for the preparation of N‐doped carbon materials. On pyrolysis under argon at 800 °C both halide precursors afforded graphite‐like structures with nitrogen contents of about 8.5 %. When the dicyanamide and tricyanomethanide precursors were thermolyzed at the same temperature, graphite‐like structures were obtained that exhibit nitrogen contents in the range 17–20 wt %; thereby, the benefit of associating a polymerizing cation with a polymerizing anion in a single precursor was demonstrated. On pyrolysis at 1100 °C the nitrogen contents of the latter pyrolysates remain high (ca. 6 wt %). Adsorption measurements with krypton at 77 K indicated that the materials are nonporous. The highest electrical conductivity was observed for a pyrolysate with one of the lowest nitrogen contents, which also has the highest degree of graphitization. Thus, the quest for N‐rich carbons with high electrical conductivities should include both maximization of the nitrogen content and optimization of the degree of graphitization. Crystallographic investigation of the precursors and spectroscopic characterization of the pyrolysates prepared by heating at 220 °C indicate that construction of the final carbon framework does not involve the intermediate formation of a polydiacetylene. Abstract : N‐riched carbon :Abstract: Imidazolium‐ and benzimidazolium‐substituted diacetylenes with bromide or nitrogen‐rich dicyanamide and tricyanomethanide anions were synthesized and used as precursors for the preparation of N‐doped carbon materials. On pyrolysis under argon at 800 °C both halide precursors afforded graphite‐like structures with nitrogen contents of about 8.5 %. When the dicyanamide and tricyanomethanide precursors were thermolyzed at the same temperature, graphite‐like structures were obtained that exhibit nitrogen contents in the range 17–20 wt %; thereby, the benefit of associating a polymerizing cation with a polymerizing anion in a single precursor was demonstrated. On pyrolysis at 1100 °C the nitrogen contents of the latter pyrolysates remain high (ca. 6 wt %). Adsorption measurements with krypton at 77 K indicated that the materials are nonporous. The highest electrical conductivity was observed for a pyrolysate with one of the lowest nitrogen contents, which also has the highest degree of graphitization. Thus, the quest for N‐rich carbons with high electrical conductivities should include both maximization of the nitrogen content and optimization of the degree of graphitization. Crystallographic investigation of the precursors and spectroscopic characterization of the pyrolysates prepared by heating at 220 °C indicate that construction of the final carbon framework does not involve the intermediate formation of a polydiacetylene. Abstract : N‐riched carbon : Azolium‐substituted diacetylenic compounds with nitrogen‐rich dicyanamide and tricyanomethanide anions undergo concomitant trimerization of the anions and polycyclization of the diacetylenic units to produce graphite‐like carbon materials (see figure). Nitrogen contents reach 17–20 wt % at 800 °C and remain as high as about 6 wt % at 1100 °C. … (more)
- Is Part Of:
- Chemistry. Volume 22:Issue 5(2016)
- Journal:
- Chemistry
- Issue:
- Volume 22:Issue 5(2016)
- Issue Display:
- Volume 22, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 22
- Issue:
- 5
- Issue Sort Value:
- 2016-0022-0005-0000
- Page Start:
- 1682
- Page End:
- 1695
- Publication Date:
- 2015-12-23
- Subjects:
- alkynes -- azolium compounds -- carbon -- cyanides -- nitrogen doping
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201502181 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9173.xml