---
res:
  bibo_abstract:
  - "<jats:p>\r\n                    C\r\n                    <jats:sub>2</jats:sub>\r\n
    \                   N‐type carbon materials are typically obtained through high‐temperature
    treatment of nitrogen‐rich molecular precursors under inert atmosphere. Herein,
    we demonstrate mechanochemical approaches that enable the synthesis of C\r\n                    <jats:sub>2</jats:sub>\r\n
    \                   N materials, namely by (i) the conversion of hexaazatriphenylenehexacarbonitrile
    (HAT‐CN) and by (ii) a one‐pot route starting from its molecular precursors, hexaketocyclohexane,
    and diaminomaleonitrile. Compared with conventional pyrolytic methods, mechanochemical
    approaches afford higher yields while significantly reducing energy input, thereby
    improving overall sustainability. The results highlight the decisive role of mechanical
    energy in directing carbon–nitrogen framework formation and demonstrate mechanochemistry
    as a versatile alternative to thermal routes for C\r\n                    <jats:sub>2</jats:sub>\r\n
    \                   N synthesis.\r\n                  </jats:p>@eng"
  bibo_authorlist:
  - foaf_Person:
      foaf_givenName: Pascal
      foaf_name: Dippner, Pascal
      foaf_surname: Dippner
  - foaf_Person:
      foaf_givenName: Sven
      foaf_name: Grätz, Sven
      foaf_surname: Grätz
  - foaf_Person:
      foaf_givenName: Jonas
      foaf_name: Lins, Jonas
      foaf_surname: Lins
  - foaf_Person:
      foaf_givenName: Torsten
      foaf_name: Gutmann, Torsten
      foaf_surname: Gutmann
      foaf_workInfoHomepage: http://www.librecat.org/personId=118165
  - foaf_Person:
      foaf_givenName: Lars
      foaf_name: Borchardt, Lars
      foaf_surname: Borchardt
  bibo_doi: 10.1002/cssc.70678
  bibo_issue: '9'
  bibo_volume: 19
  dct_date: 2026^xs_gYear
  dct_isPartOf:
  - http://id.crossref.org/issn/1864-5631
  - http://id.crossref.org/issn/1864-564X
  dct_language: eng
  dct_publisher: Wiley@
  dct_title: Mechanochemical Near‐Ambient Synthesis of C                    <sub>2</sub>                    N
    Materials From HAT‐CN and its Precursors@
...