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词条 Carbon nitride
释义

  1. Covalent network compounds

  2. Azafullerenes

  3. Cyanofullerenes

  4. Cyanogen

  5. Percyanoalkynes, -alkenes and -alkanes

      Dicyanopolyynes  

  6. Perazidoalkynes, -alkenes and -alkanes

  7. Percyanoheterocycles

  8. Aromatic cyanocarbons

  9. Other compounds

  10. Anions

  11. See also

  12. References

Carbon nitrides are compounds of carbon and nitrogen.

Covalent network compounds

  • Beta carbon nitride - a solid with a formula β-C3N4, which is predicted to be harder than diamond.
  • Graphitic carbon nitride - g-C3N4, with important catalytic properties

Azafullerenes

  • Azafullerenes are a class of heterofullerenes in which the element substituting for carbon is nitrogen.[1] Examples include (C59N)2 (biazafullerenyl),[2] C58N2 (diaza[60]fullerene), C57N3 (triaza[60]fullerene) and C48N12.

Cyanofullerenes

  • Cyanofullerenes are a class of modified fullerenes in which cyano- groups are attached to a fullerene skeleton. These have the formula C60(CN)2n, where n takes the values 1 to 9.

Cyanogen

  • Cyanogen - C2N2 (NCCN)
  • Isocyanogen - C2N2 (CNCN)
  • Paracyanogen - a cyanogen polymer, (NCCN)n
  • Paraisocyanogen - a cyanogen polymer, (CNCN)n

Percyanoalkynes, -alkenes and -alkanes

  • dicyanoacetylene - C4N2 [C2(CN)2], also called carbon subnitride or but-2-ynedinitrile
  • tetracyanoethylene - C6N4 [C2(CN)4]
  • tetracyanomethane - C5N4 [C(CN)4]
    • 2,2-diisocyanopropanedinitrile - C5N4 [C(CN)2(NC)2]
  • hexacyanoethane - C8N6 [C2(CN)6]
  • hexacyanocyclopropane - C9N6 [C3(CN)6]
  • hexacyanobutadiene[3] - C10N6 [C4(CN)6]

Dicyanopolyynes

Dicyanopolyynes are composed of a chain of carbon atoms with alternating single and triple bonds, terminated by nitrogen atoms. Although not a polyyne dicyanoacetylene otherwise fits within this series.

  • dicyanobutadiyne (dicyanodiacetylene)- C6N2
  • dicyanohexatriyne - C8N2
  • C10N2
  • C12N2
  • C14N2
  • C16N2
  • C18N2
  • C20N2
  • C22N2

Perazidoalkynes, -alkenes and -alkanes

  • tetraazidomethane - CN12

Percyanoheterocycles

  • pentacyanopyridine - C10N6
  • tetracyanopyrazine - C8N6
  • tricyanotriazine - C6N6[4]
  • tetracyano-bitriazine - C10N10[4]
  • dicyanotetrazine - C4N6
  • hexacyanotrisimidazole - C15N12
  • hexacyanohexaazatriphenylene - C18N12

Aromatic cyanocarbons

  • hexacyanobenzene - C12N6
  • octacyanonaphthalene - C18N8
  • decacyanoanthracene - C24N10

Other compounds

  • cyanonitrene - CN2 [NCN]
  • azodicarbonitrile - C2N4 [(NCN)2]
  • cyanogen azide - CN4 [NC.N3]
  • 1-diazidocarbamoyl-5-azidotetrazole - C2N14
  • triazidotriazine (cyanuric triazide) - C3N12 [C3N3(N3)3]
  • triazidoheptazine - C6N16 [C6N7(N3)3]
  • tricyanomethanimine (Dicyanomethylene-cyanamide) - C4N4 [(CN).N.C(CN)2]
  • diazidodicyanoethylene - C4N8 [(N3)2.C.C(CN)2]
  • dicyanodiazomethane - C3N4 [(CN)2.C.N2]
  • dicyanocarbene - C3N2 (and isomers cyanoisocyanocarbene, diisocyanocarbene, 3-cyano-2H-azirenylidene and 3-isocyano-2H-azirenylidene)
  • 1,3,5-triazido-2,4,6-tricyanobenzene - C9N12 [C6(CN)3(N3)3]
  • nitrogen tricyanide N(CN)3 and carbon bis(cyanamide) NCN=C=NCN, two formal monomers of polymeric C3N4

Anions

  • cyanide and isocyanide - CN and NC
  • dicyanamide - N(CN)2
  • tricyanomethanide - C(CN)3
  • pentacyanoethanide - C2(CN)5
  • pentacyanopropenide (pentacyanoallyl anion) - C3(CN)5
  • 2-dicyanomethylene-1,1,3,3-tetracyanopropanediide C10N62− [(C(C(CN)2)32−]
  • tricyanomelaminate anion - C3N3(NCN)3]3−
  • melonate - C6N7(NCN)3]3−
  • cyanofullerene anions - C60(CN)n (n odd) and C60(CN)n2− (n even)
  • cyanopolyynide anions - CnN (n odd)
    • cyanoacetlyide - C3N
    • cyanobutadiynylide - C5N

See also

  • Oxocarbon

References

1. ^D.J. Harris, Discovery of Nitroballs: Research in Fullerene Chemistry, 1993 California State Science Fair, http://www.usc.edu/CSSF/History/1993/S05.html
2. ^Hummelen et al, Isolation of the Heterofullerene C59N as Its Dimer (C59N)2, Science 269: 1554-1556 (1995)
3. ^O.W.Webster, Hexacyanobutadiene, J. Am. Chem. Soc. 86(14): 2898–2902 (1964)
4. ^Sesto et al, Chemical Reduction of 2,4,6-Tricyano-1,3,5-triazine and 1,3,5-Tricyanobenzene. Formation of Novel 4,4',6,6'-Tetracyano-2,2'-bitriazine and Its Radical Anion, J. Org. Chem. 68: 3367-3379 (2003)
{{carbon compounds}}

1 : Carbon compounds

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