A carbon–nitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry.[1]

Nitrogen has five valence electrons and in simple amines it is trivalent, with the two remaining electrons forming a lone pair. Through that pair, nitrogen can form an additional bond to hydrogen making it tetravalent and with a positive charge in ammonium salts. Many nitrogen compounds can thus be potentially basic but its degree depends on the configuration: the nitrogen atom in amides is not basic due to delocalization of the lone pair into a double bond and in pyrrole the lone pair is part of an aromatic sextet.

Similar to carbon–carbon bonds, these bonds can form stable double bonds, as in imines; and triple bonds, such as nitriles. Bond lengths range from 147.9 pm for simple amines to 147.5 pm for C-N= compounds such as nitromethane to 135.2 pm for partial double bonds in pyridine to 115.8 pm for triple bonds as in nitriles.[2]

A CN bond is strongly polarized towards nitrogen (the electronegativities of C and N are 2.55 and 3.04, respectively) and subsequently molecular dipole moments can be high: cyanamide 4.27 D, diazomethane 1.5 D, methyl azide 2.17, pyridine 2.19. For this reason many compounds containing CN bonds are water-soluble. N-philes are group of radical molecules which are specifically attracted to the C=N bonds.[3]

Carbon-nitrogen bond can be analyzed by X-ray photoelectron spectroscopy (XPS). Depending on the bonding states the peak positions differ in N1s XPS spectra.[4][5][6]

Nitrogen functional groups

Chemical class Bond order Formula Structural Formula Example Avg. C–N bond length (Å)[7]
Amines1 R2C-NH2 Primary amine methylamine
Methylamine
 1.469 (neutral amine)
1.499 (ammonium salt)
Aziridines1 CH2NHCH2 Aziridine Mitomycin
Mitomycin
 1.472
Azides1 R2C-N3 Azide Phenyl azide
Phenyl azide
 1.38–1.48[8]
1.47 (methyl azide)[9]
1.432 (phenyl azide)[10]
Anilines1 Ph-NH2 Aniline Ansidine
Anisidine		 1.355 (sp2 N)
1.395 (sp3 N)
1.465 (ammonium salt)
Pyrroles1 amide Porphyrin
Porphyrin		 1.372
Amides1.2 R-CO-NR2 amide Acetamide
Acetamide		 1.325 (primary)
1.334 (secondary)
1.346 (tertiary)
Pyridines1.5 pyr pyridine Nicotinamide
Nicotinamide		 1.337
Imines2 R2C=NR imine DBN
DBN		 1.279 (C=N bond)
1.465 (C–N bond)
Nitriles3 R-CN Nitrile Benzonitrile
Benzonitrile		 1.136
Isonitriles3 R-NC isonitrile TOSMIC
TOSMIC		 1.154[11]

See also

References

  1. ↑ Organic Chemistry John McMurry 2nd Ed.
  2. ↑ CRC Handbook of Chemistry and Physics 65Th Ed.
  3. ↑ Falzon, Chantal T.; Ryu, Ilhyong; Schiesser, Carl H. (2002). "5-Azahexenoyl radicals cyclize via nucleophilic addition to the acyl carbon rather than 5-exo homolytic addition at the imine". Chemical Communications (20): 2338–9. doi:10.1039/B207729A. PMID 12430429.
  4. ↑ Kato, Tomofumi; Yamada, Yasuhiro; Nishikawa, Yasushi; Otomo, Toshiya; Sato, Hayato; Sato, Satoshi (2021-07-12). "Origins of peaks of graphitic and pyrrolic nitrogen in N1s X-ray photoelectron spectra of carbon materials: quaternary nitrogen, tertiary amine, or secondary amine?". Journal of Materials Science. 56 (28): 15798–15811. doi:10.1007/s10853-021-06283-5. ISSN 1573-4803. S2CID 235793266.
  5. ↑ Yamada, Yasuhiro; Kim, Jungpil; Matsuo, Shintaro; Sato, Satoshi (2014-04-01). "Nitrogen-containing graphene analyzed by X-ray photoelectron spectroscopy". Carbon. 70: 59–74. doi:10.1016/j.carbon.2013.12.061. ISSN 0008-6223.
  6. ↑ Yamada, Yasuhiro; Tanaka, Haruki; Kubo, Shingo; Sato, Satoshi (2021-09-01). "Unveiling Bonding States and Roles of Edges in Nitrogen-Doped Graphene Nanoribbon by X-ray Photoelectron Spectroscopy". Carbon. 185: 342–367. doi:10.1016/j.carbon.2021.08.085. ISSN 0008-6223. S2CID 239687362.
  7. ↑ F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen. Tables of bond Lengths determined by X-Ray and Neutron Diffraction. Part 1. Bond Lengths in Organic Compounds. J. Chem. Soc. Perkin Trans. II 1987, S1-S19.
  8. ↑ Kumasaki, M.; Kinbara, K.; Wada, Y.; Arai, M.; Tamura, M. (2001). "Azidoacetamide, a neutral small organic azide". Acta Crystallogr. E. 57: o6–o8. doi:10.1107/S160053680001850X.
  9. ↑ Livingston, R. L.; Rao, C. N. Ramachandra (1960). "An Electron Diffraction Investigation of the Molecular Structure of Methyl Azide". J. Phys. Chem. 64 (6): 756–759. doi:10.1021/j100835a012.
  10. ↑ Wagner, Gerald; Arion, Vladimir B.; Brecker, Lothar; Krantz, Carsten; Mieusset, Jean-Luc; Brinker, Udo H. (2009). "Controllable Selective Functionalization of a Cavitand via Solid State Photolysis of an Encapsulated Phenyl Azide". Org. Lett. 11 (14): 3056–3058. doi:10.1021/ol901122h. PMID 19537769.
  11. ↑ Bano, Huma; Yousuf, Sammer (2015). "Crystal structure of p-toluenesulfonylmethyl isocyanide". Acta Crystallogr. E. 71 (6): o412. doi:10.1107/S2056989015008816. PMC 4459310. PMID 26090196. S2CID 26154257.
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