Aniline (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Aniline" in English language version.

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archive.org

August Wilhelm Hofmann (1843) "Chemische Untersuchung der organischen Basen im Steinkohlen-Theeröl" (Chemical investigation of organic bases in coal tar oil), Annalen der Chemie und Pharmacie, 47: 37–87. On page 48, Hofmann argues that krystallin, kyanol, benzidam, and aniline are identical.

archive.today

"Aniline". The Chemical Market Reporter. Archived from the original on 2002-02-19. Retrieved 2007-12-21.

bnf.fr

gallica.bnf.fr

A. Béchamp (1854) "De l'action des protosels de fer sur la nitronaphtaline et la nitrobenzine. Nouvelle méthode de formation des bases organiques artificielles de Zinin" (On the action of iron protosalts on nitronaphthaline and nitrobenzene. New method of forming Zinin's synthetic organic bases.), Annales de Chemie et de Physique, 3rd series, 42: 186 – 196. (Note: In the case of a metal having two or more distinct oxides (e.g., iron), a "protosalt" is an obsolete term for a salt that is obtained from the oxide containing the lowest proportion of oxygen to metal; e.g., in the case of iron, which has two oxides – iron (II) oxide (FeO) and iron (III) oxide (Fe₂O₃) – FeO is the "protoxide" from which protosalts can be made. See: Wiktionary: protosalt.)

books.google.com

Kahl, Thomas; Schröder, K. W.; Lawrence, F. R.; Elvers, Barbara; Höke, Hartmut; Pfefferkorn, R.; Marshall, W. J. (2007). "Aniline". In Ullmann, Fritz (ed.). Ullmann's encyclopedia of industrial chemistry. Wiley: New York. doi:10.1002/14356007.a02_303. ISBN 978-3-527-20138-9. OCLC 11469727.
Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
Otto Unverdorben (1826). "Ueber das Verhalten der organischen Körper in höheren Temperaturen" [On the behaviour of organic substances at high temperatures]. Annalen der Physik und Chemie. 8 (11): 397–410. Bibcode:1826AnP....84..397U. doi:10.1002/andp.18260841109.
F. F. Runge (1834) "Ueber einige Produkte der Steinkohlendestillation" (On some products of coal distillation), Annalen der Physik und Chemie, 31: 65–77 (see page 65), 513–524; and 32: 308–332 (see page 331).
F. F. Runge (1834) "Ueber einige Produkte der Steinkohlendestillation" (On some products of coal distillation), Annalen der Physik und Chemie, 31: 65–77 (see page 65), 513–524; and 32: 308–332 (see page 331).
N. Zinin (1842). "Beschreibung einiger neuer organischer Basen, dargestellt durch die Einwirkung des Schwefelwasserstoffes auf Verbindungen der Kohlenwasserstoffe mit Untersalpetersäure" (Description of some new organic bases, produced by the action of hydrogen sulfide on compounds of hydrocarbons and hyponitric acid [H₂N₂O₃]), Bulletin Scientifique [publié par l'Académie Impériale des Sciences de Saint-Petersbourg], 10 (18): 272–285. Reprinted in: N. Zinin (1842) "Beschreibung einiger neuer organischer Basen, dargestellt durch die Einwirkung des Schwefelwasserstoffes auf Verbindungen der Kohlenwasserstoffe mit Untersalpetersäure", Journal für praktische Chemie, 27 (1): 140–153. Benzidam is named on page 150. Fritzsche, Zinin's colleague, soon recognized that "benzidam" was actually aniline. See: Fritzsche (1842) Bulletin Scientifique, 10: 352. Reprinted as a postscript to Zinin's article in: J. Fritzsche (1842) "Bemerkung zu vorstehender Abhandlung des Hrn. Zinin" (Comment on the preceding article by Mr. Zinin), Journal für praktische Chemie, 27 (1): 153.
See also: (Anon.) (1842) "Organische Salzbasen, aus Nitronaphtalose und Nitrobenzid mittelst Schwefelwasserstoff entstehend" (Organic bases originating from nitronaphthalene and nitrobenzene via hydrogen sulfide), Annalen der Chemie und Pharmacie, 44: 283–287.
Perkin, William Henry. 1861-06-08. "Proceedings of Chemical Societies: Chemical Society, Thursday, May 16, 1861". The Chemical News and Journal of Industrial Science. Retrieved on 2007-09-24.
Auerbach G, "Azo and naphthol dyes", Textile Colorist, 1880 May;2(17):137-9, p 138.
Wilcox RW, "The treatment of influenza in adults", Medical News, 1900 Dec 15;77():931-2, p 932.
D J Th Wagener, The History of Oncology (Houten: Springer, 2009), pp 150–1.
John E Lesch, The First Miracle Drugs: How the Sulfa Drugs Transformed Medicine (New York: Oxford University Press, 2007), pp 202–3.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0033". National Institute for Occupational Safety and Health (NIOSH).
"Aniline". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

doi.org

Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 416, 668. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. Aniline, for C₆H₅-NH₂, is the only name for a primary amine retained as a preferred IUPAC name for which full substitution is permitted on the ring and the nitrogen atom. It is a Type 2a retained name; for the rules of substitution see P-15.1.8.2. Substitution is limited to substituent groups cited as prefixes in accordance with the seniority of functional groups explicitly expressed or implied in the functional parent compound name. The name benzenamine may be used in general nomenclature.
Kahl, Thomas; Schröder, K. W.; Lawrence, F. R.; Elvers, Barbara; Höke, Hartmut; Pfefferkorn, R.; Marshall, W. J. (2007). "Aniline". In Ullmann, Fritz (ed.). Ullmann's encyclopedia of industrial chemistry. Wiley: New York. doi:10.1002/14356007.a02_303. ISBN 978-3-527-20138-9. OCLC 11469727.
Zhang, Huaiyu; Jiang, Xiaoyu; Wu, Wei; Mo, Yirong (April 28, 2016). "Electron conjugation versus π-π repulsion in substituted benzenes: why the carbon-nitrogen bond in nitrobenzene is longer than in aniline". Physical Chemistry Chemical Physics. 18 (17): 11821–11828. Bibcode:2016PCCP...1811821Z. doi:10.1039/c6cp00471g. ISSN 1463-9084. PMID 26852720.
Raczyńska, Ewa D.; Hallman, Małgorzata; Kolczyńska, Katarzyna; Stępniewski, Tomasz M. (2010-07-12). "On the Harmonic Oscillator Model of Electron Delocalization (HOMED) Index and its Application to Heteroatomic π-Electron Systems". Symmetry. 2 (3): 1485–1509. Bibcode:2010Symm....2.1485R. doi:10.3390/sym2031485. ISSN 2073-8994.
G. M. Wójcik "Structural Chemistry of Anilines" in Anilines (Patai's Chemistry of Functional Groups), S. Patai, Ed. 2007, Wiley-VCH, Weinheim. doi:10.1002/9780470682531.pat0385.
Sorriso, S. (1982). "Structural chemistry". Amino, Nitrosco and Nitro Compounds and Their Derivatives: Vol. 1 (1982). pp. 1–51. doi:10.1002/9780470771662.ch1. ISBN 9780470771662.
Westerhaus, Felix A.; Jagadeesh, Rajenahally V.; Wienhöfer, Gerrit; Pohl, Marga-Martina; Radnik, Jörg; Surkus, Annette-Enrica; Rabeah, Jabor; Junge, Kathrin; Junge, Henrik; Nielsen, Martin; Brückner, Angelika; Beller, Matthias (2013). "Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes". Nature Chemistry. 5 (6): 537–543. Bibcode:2013NatCh...5..537W. doi:10.1038/nchem.1645. PMID 23695637. S2CID 3273484.
Porter, H. K. (2011), "The Zinin Reduction of Nitroarenes", Organic Reactions, John Wiley & Sons, Ltd, pp. 455–481, doi:10.1002/0471264180.or020.04, ISBN 978-0-471-26418-7, retrieved 2022-02-01
Jung, Woo-Hyuk; Ha, Eun-Ju; Chung, Il doo; Lee, Jang-Oo (2008-08-01). "Synthesis of aniline-based azopolymers for surface relief grating". Macromolecular Research. 16 (6): 532–538. doi:10.1007/BF03218555. ISSN 2092-7673. S2CID 94372490.
Otto Unverdorben (1826). "Ueber das Verhalten der organischen Körper in höheren Temperaturen" [On the behaviour of organic substances at high temperatures]. Annalen der Physik und Chemie. 8 (11): 397–410. Bibcode:1826AnP....84..397U. doi:10.1002/andp.18260841109.
Wainwright, Mark (January 2008). "Dyes in the development of drugs and pharmaceuticals". Dyes and Pigments. 76 (3): 582–589. doi:10.1016/j.dyepig.2007.01.015.
Tanaka, Takuji; Miyazawa, Katsuhito; Tsukamoto, Testuya; Kuno, Toshiya; Suzuki, Koji (2011). "Pathobiology and Chemoprevention of Bladder Cancer". Journal of Oncology. 2011: 1–23. doi:10.1155/2011/528353. PMID 21941546.
Ma, Huaxian; Wang, Jianling; Abdel-Rahman, Sherif Z.; Boor, Paul J.; Khan, M. Firoze (2008). "Oxidative DNA damage and its repair in rat spleen following subchronic exposure to aniline". Toxicology and Applied Pharmacology. 233 (2): 247–253. doi:10.1016/j.taap.2008.08.010. PMC 2614128. PMID 18793663.

dx.doi.org

Alabugin I. V.; Manoharan, M.; Buck, M.; Clark, R. J. Substituted Anilines: The Tug-Of-War between Pyramidalization and Resonance Inside and Outside of Crystal Cavities. THEOCHEM, 2007, 813, 21-27. http://dx.doi.org/10.1016/j.theochem.2007.02.016.

etymonline.com

"aniline | Etymology, origin and meaning of aniline by etymonline". www.etymonline.com. Retrieved 2022-02-15.
synonym I anil, ultimately from Sanskrit "nīla", dark-blue.

harvard.edu

ui.adsabs.harvard.edu

Zhang, Huaiyu; Jiang, Xiaoyu; Wu, Wei; Mo, Yirong (April 28, 2016). "Electron conjugation versus π-π repulsion in substituted benzenes: why the carbon-nitrogen bond in nitrobenzene is longer than in aniline". Physical Chemistry Chemical Physics. 18 (17): 11821–11828. Bibcode:2016PCCP...1811821Z. doi:10.1039/c6cp00471g. ISSN 1463-9084. PMID 26852720.
Raczyńska, Ewa D.; Hallman, Małgorzata; Kolczyńska, Katarzyna; Stępniewski, Tomasz M. (2010-07-12). "On the Harmonic Oscillator Model of Electron Delocalization (HOMED) Index and its Application to Heteroatomic π-Electron Systems". Symmetry. 2 (3): 1485–1509. Bibcode:2010Symm....2.1485R. doi:10.3390/sym2031485. ISSN 2073-8994.
Westerhaus, Felix A.; Jagadeesh, Rajenahally V.; Wienhöfer, Gerrit; Pohl, Marga-Martina; Radnik, Jörg; Surkus, Annette-Enrica; Rabeah, Jabor; Junge, Kathrin; Junge, Henrik; Nielsen, Martin; Brückner, Angelika; Beller, Matthias (2013). "Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes". Nature Chemistry. 5 (6): 537–543. Bibcode:2013NatCh...5..537W. doi:10.1038/nchem.1645. PMID 23695637. S2CID 3273484.
Otto Unverdorben (1826). "Ueber das Verhalten der organischen Körper in höheren Temperaturen" [On the behaviour of organic substances at high temperatures]. Annalen der Physik und Chemie. 8 (11): 397–410. Bibcode:1826AnP....84..397U. doi:10.1002/andp.18260841109.

nih.gov

pubmed.ncbi.nlm.nih.gov

Zhang, Huaiyu; Jiang, Xiaoyu; Wu, Wei; Mo, Yirong (April 28, 2016). "Electron conjugation versus π-π repulsion in substituted benzenes: why the carbon-nitrogen bond in nitrobenzene is longer than in aniline". Physical Chemistry Chemical Physics. 18 (17): 11821–11828. Bibcode:2016PCCP...1811821Z. doi:10.1039/c6cp00471g. ISSN 1463-9084. PMID 26852720.
Westerhaus, Felix A.; Jagadeesh, Rajenahally V.; Wienhöfer, Gerrit; Pohl, Marga-Martina; Radnik, Jörg; Surkus, Annette-Enrica; Rabeah, Jabor; Junge, Kathrin; Junge, Henrik; Nielsen, Martin; Brückner, Angelika; Beller, Matthias (2013). "Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes". Nature Chemistry. 5 (6): 537–543. Bibcode:2013NatCh...5..537W. doi:10.1038/nchem.1645. PMID 23695637. S2CID 3273484.
Tanaka, Takuji; Miyazawa, Katsuhito; Tsukamoto, Testuya; Kuno, Toshiya; Suzuki, Koji (2011). "Pathobiology and Chemoprevention of Bladder Cancer". Journal of Oncology. 2011: 1–23. doi:10.1155/2011/528353. PMID 21941546.
Ma, Huaxian; Wang, Jianling; Abdel-Rahman, Sherif Z.; Boor, Paul J.; Khan, M. Firoze (2008). "Oxidative DNA damage and its repair in rat spleen following subchronic exposure to aniline". Toxicology and Applied Pharmacology. 233 (2): 247–253. doi:10.1016/j.taap.2008.08.010. PMC 2614128. PMID 18793663.

ncbi.nlm.nih.gov

Ma, Huaxian; Wang, Jianling; Abdel-Rahman, Sherif Z.; Boor, Paul J.; Khan, M. Firoze (2008). "Oxidative DNA damage and its repair in rat spleen following subchronic exposure to aniline". Toxicology and Applied Pharmacology. 233 (2): 247–253. doi:10.1016/j.taap.2008.08.010. PMC 2614128. PMID 18793663.

noaa.gov

cameochemicals.noaa.gov

"Aniline". cameochemicals.noaa.gov. US NOAA Office of Response and Restoration. Retrieved 2016-06-16.

nuclear-weapons.info

Brian Burnell. 2016. http://www.nuclear-weapons.info/cde.htm#Corporal SSM

organic-chemistry.org

"Aniline synthesis by amination (Arylation)".

orgsyn.org

Carl N. Webb (1941). "Benzanilide". Organic Syntheses; Collected Volumes, vol. 1, p. 82.

patents.google.com

US3136818A, Heinrich, Sperber; Guenter, Poehler & Joachim, Pistor Hans et al., "Production of aniline", issued 1964-06-09

semanticscholar.org

api.semanticscholar.org

Westerhaus, Felix A.; Jagadeesh, Rajenahally V.; Wienhöfer, Gerrit; Pohl, Marga-Martina; Radnik, Jörg; Surkus, Annette-Enrica; Rabeah, Jabor; Junge, Kathrin; Junge, Henrik; Nielsen, Martin; Brückner, Angelika; Beller, Matthias (2013). "Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes". Nature Chemistry. 5 (6): 537–543. Bibcode:2013NatCh...5..537W. doi:10.1038/nchem.1645. PMID 23695637. S2CID 3273484.
Jung, Woo-Hyuk; Ha, Eun-Ju; Chung, Il doo; Lee, Jang-Oo (2008-08-01). "Synthesis of aniline-based azopolymers for surface relief grating". Macromolecular Research. 16 (6): 532–538. doi:10.1007/BF03218555. ISSN 2092-7673. S2CID 94372490.

the-innovation-group.com

"Aniline". The Chemical Market Reporter. Archived from the original on 2002-02-19. Retrieved 2007-12-21.

time.com

"Medicine: Spoils of War". Time. 15 May 1950. Archived from the original on 24 June 2013. Retrieved 20 November 2020.

web.archive.org

"Medicine: Spoils of War". Time. 15 May 1950. Archived from the original on 24 June 2013. Retrieved 20 November 2020.

wiktionary.org

en.wiktionary.org

A. Béchamp (1854) "De l'action des protosels de fer sur la nitronaphtaline et la nitrobenzine. Nouvelle méthode de formation des bases organiques artificielles de Zinin" (On the action of iron protosalts on nitronaphthaline and nitrobenzene. New method of forming Zinin's synthetic organic bases.), Annales de Chemie et de Physique, 3rd series, 42: 186 – 196. (Note: In the case of a metal having two or more distinct oxides (e.g., iron), a "protosalt" is an obsolete term for a salt that is obtained from the oxide containing the lowest proportion of oxygen to metal; e.g., in the case of iron, which has two oxides – iron (II) oxide (FeO) and iron (III) oxide (Fe₂O₃) – FeO is the "protoxide" from which protosalts can be made. See: Wiktionary: protosalt.)

wiley.com

onlinelibrary.wiley.com

Porter, H. K. (2011), "The Zinin Reduction of Nitroarenes", Organic Reactions, John Wiley & Sons, Ltd, pp. 455–481, doi:10.1002/0471264180.or020.04, ISBN 978-0-471-26418-7, retrieved 2022-02-01

worldcat.org

search.worldcat.org

Kahl, Thomas; Schröder, K. W.; Lawrence, F. R.; Elvers, Barbara; Höke, Hartmut; Pfefferkorn, R.; Marshall, W. J. (2007). "Aniline". In Ullmann, Fritz (ed.). Ullmann's encyclopedia of industrial chemistry. Wiley: New York. doi:10.1002/14356007.a02_303. ISBN 978-3-527-20138-9. OCLC 11469727.
Zhang, Huaiyu; Jiang, Xiaoyu; Wu, Wei; Mo, Yirong (April 28, 2016). "Electron conjugation versus π-π repulsion in substituted benzenes: why the carbon-nitrogen bond in nitrobenzene is longer than in aniline". Physical Chemistry Chemical Physics. 18 (17): 11821–11828. Bibcode:2016PCCP...1811821Z. doi:10.1039/c6cp00471g. ISSN 1463-9084. PMID 26852720.
Raczyńska, Ewa D.; Hallman, Małgorzata; Kolczyńska, Katarzyna; Stępniewski, Tomasz M. (2010-07-12). "On the Harmonic Oscillator Model of Electron Delocalization (HOMED) Index and its Application to Heteroatomic π-Electron Systems". Symmetry. 2 (3): 1485–1509. Bibcode:2010Symm....2.1485R. doi:10.3390/sym2031485. ISSN 2073-8994.
Alabugin, Igor V. (2016). Stereoelectronic effects : a bridge between structure and reactivity. Chichester, UK. ISBN 978-1-118-90637-8. OCLC 957525299.{{cite book}}: CS1 maint: location missing publisher (link)
Carey, Francis A. (2008). Organic chemistry (7th ed.). Boston: McGraw-Hill Higher Education. ISBN 9780073047874. OCLC 71790138.
Jung, Woo-Hyuk; Ha, Eun-Ju; Chung, Il doo; Lee, Jang-Oo (2008-08-01). "Synthesis of aniline-based azopolymers for surface relief grating". Macromolecular Research. 16 (6): 532–538. doi:10.1007/BF03218555. ISSN 2092-7673. S2CID 94372490.