Бензен (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Бензен" in Serbian language version.
refsWebsite
Global rank
Serbian rank
3rd place
2nd place
18th place
28th place
149th place
283rd place
low place
low place
8,036th place
2,763rd place
924th place
1,411th place
6th place
5th place
archive.org
- The word "benzoin" is derived from the Arabic expression "luban jawi", or "frankincense of Java". Morris, Edwin T. (1984). Fragrance: The Story of Perfume from Cleopatra to Chanel. Charles Scribner's Sons. стр. 101. ISBN 978-0684181950.
bnf.fr
gallica.bnf.fr
- Faraday, M. (1825). „On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat”. Philosophical Transactions of the Royal Society. 115: 440—466. JSTOR 107752. doi:10.1098/rstl.1825.0022. On pages 443–450, Faraday discusses "bicarburet of hydrogen" (benzene). On pages 449–450, he shows that benzene's empirical formula is C6H6, although he doesn't realize it because he (like most chemists at that time) used the wrong atomic mass for carbon (6 instead of 12).
books.google.com
- Coker, A. Kayode; Ludwig, Ernest E. (2007). Ludwig's Applied Process Design for Chemical And Petrochemical Plants. 1. Elsevier. стр. 114. ISBN 978-0-7506-7766-0. Приступљено 31. 05. 2012.
- Atherton Seidell; William F. Linke (1952). Solubilities of Inorganic and Organic Compounds: A Compilation of Solubility Data from the Periodical Literature. Supplement. Van Nostrand.
- Mitscherlich, E. (1834). „Über das Benzol und die Säuren der Oel- und Talgarten” [On benzol and oily and fatty types of acids]. Annalen der Pharmacie. 9 (1): 39—48. doi:10.1002/jlac.18340090103. In a footnote on page 43, Liebig, the journal's editor, suggested changing Mitscherlich's original name for benzene (namely, "benzin") to "benzol", because the suffix "-in" suggested that it was an alkaloid (e.g., Chinin (quinine)), which benzene isn't, whereas the suffix "-ol" suggested that it was oily, which benzene is. Thus on page 44, Mitscherlich states: "Da diese Flüssigkeit aus der Benzoësäure gewonnen wird, und wahrscheinlich mit den Benzoylverbindungen im Zusammenhang steht, so gibt man ihr am besten den Namen Benzol, da der Name Benzoïn schon für die mit dem Bittermandelöl isomerische Verbindung von Liebig und Wöhler gewählt worden ist." (Since this liquid [benzene] is obtained from benzoic acid and probably is related to benzoyl compounds, the best name for it is "benzol", since the name "benzoïn" has already been chosen, by Liebig and Wöhler, for the compound that's isomeric with the oil of bitter almonds [benzaldehyde].)
- Laurent, Auguste (1836). „Sur la chlorophénise et les acides chlorophénisique et chlorophénèsique”. Annales de Chemie et de Physique. 63: 27—45., see p. 44: "Je donne le nom de phène au radical fondamental des acides précédens (φαινω, j'éclaire), puisque la benzine se trouve dans le gaz de l'éclairage." (I give the name of "phène" (φαινω, I illuminate) to the fundamental radical of the preceding acids, because benzene is found in illuminating gas.)
- Hofmann, A. W. (1845) „Ueber eine sichere Reaction auf Benzol”. Annalen der Chemie und Pharmacie. 55: 200—205. (On a reliable test for benzene), ; on pp. 204–205, Hofmann found benzene in coal tar oil.
- Mansfield Charles Blachford (1849). „Untersuchung des Steinkohlentheers”. Annalen der Chemie und Pharmacie. 69 (2): 162—180. doi:10.1002/jlac.18490690203.
cdc.gov
- NIOSH Џепни водич хемијских хазарда. „#0049”. Nacionalni institut za bezbednost i zdravlje na radu (NIOSH).
- „Benzene”. Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
chemister.ru
doi.org
- Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. стр. 10, 22, 204, 494, 577. ISBN 978-0-85404-182-4. doi:10.1039/9781849733069.
- Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
- Arnold, D.; Plank, C.; Erickson, E.; Pike, F. (1958). „Solubility of Benzene in Water”. Industrial & Engineering Chemistry Chemical & Engineering Data Series. 3 (2): 253—256. doi:10.1021/i460004a016.
- Breslow, R.; Guo, T. (1990). „Surface tension measurements show that chaotropic salting-in denaturants are not just water-structure breakers”. Proceedings of the National Academy of Sciences of the United States of America. 87 (1): 167—9. Bibcode:1990PNAS...87..167B. PMC 53221
. PMID 2153285. doi:10.1073/pnas.87.1.167. - Rocke, A. J. (1985). „Hypothesis and Experiment in the Early Development of Kekule's Benzene Theory”. Annals of Science. 42 (4): 355—81. doi:10.1080/00033798500200411.
- Faraday, M. (1825). „On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat”. Philosophical Transactions of the Royal Society. 115: 440—466. JSTOR 107752. doi:10.1098/rstl.1825.0022. On pages 443–450, Faraday discusses "bicarburet of hydrogen" (benzene). On pages 449–450, he shows that benzene's empirical formula is C6H6, although he doesn't realize it because he (like most chemists at that time) used the wrong atomic mass for carbon (6 instead of 12).
- Kaiser, R. (1968). „Bicarburet of Hydrogen. Reappraisal of the Discovery of Benzene in 1825 with the Analytical Methods of 1968”. Angewandte Chemie International Edition in English. 7 (5): 345—350. doi:10.1002/anie.196803451.
- Mitscherlich, E. (1834). „Über das Benzol und die Säuren der Oel- und Talgarten” [On benzol and oily and fatty types of acids]. Annalen der Pharmacie. 9 (1): 39—48. doi:10.1002/jlac.18340090103. In a footnote on page 43, Liebig, the journal's editor, suggested changing Mitscherlich's original name for benzene (namely, "benzin") to "benzol", because the suffix "-in" suggested that it was an alkaloid (e.g., Chinin (quinine)), which benzene isn't, whereas the suffix "-ol" suggested that it was oily, which benzene is. Thus on page 44, Mitscherlich states: "Da diese Flüssigkeit aus der Benzoësäure gewonnen wird, und wahrscheinlich mit den Benzoylverbindungen im Zusammenhang steht, so gibt man ihr am besten den Namen Benzol, da der Name Benzoïn schon für die mit dem Bittermandelöl isomerische Verbindung von Liebig und Wöhler gewählt worden ist." (Since this liquid [benzene] is obtained from benzoic acid and probably is related to benzoyl compounds, the best name for it is "benzol", since the name "benzoïn" has already been chosen, by Liebig and Wöhler, for the compound that's isomeric with the oil of bitter almonds [benzaldehyde].)
- Mansfield Charles Blachford (1849). „Untersuchung des Steinkohlentheers”. Annalen der Chemie und Pharmacie. 69 (2): 162—180. doi:10.1002/jlac.18490690203.
- Hoffman, Augustus W. (1856). „On insolinic acid”. Proceedings of the Royal Society. 8: 1—3. doi:10.1098/rspl.1856.0002. „The existence and mode of formation of insolinic acid prove that to the series of monobasic aromatic acids, Cn2Hn2-8O4, the lowest known term of which is benzoic acid, … .” [Note: The empirical formulas of organic compounds that appear in Hofmann's article (p. 3) are based upon an atomic mass of carbon of 6 (instead of 12) and an atomic mass of oxygen of 8 (instead of 16).]
- Cernicharo, José; et al. (1997), „Infrared Space Observatory's Discovery of C4H2, C6H2, and Benzene in CRL 618”, Astrophysical Journal Letters, 546 (2): L123—L126, Bibcode:2001ApJ...546L.123C, doi:10.1086/318871
harvard.edu
adsabs.harvard.edu
- Breslow, R.; Guo, T. (1990). „Surface tension measurements show that chaotropic salting-in denaturants are not just water-structure breakers”. Proceedings of the National Academy of Sciences of the United States of America. 87 (1): 167—9. Bibcode:1990PNAS...87..167B. PMC 53221 . PMID 2153285. doi:10.1073/pnas.87.1.167.
- Cernicharo, José; et al. (1997), „Infrared Space Observatory's Discovery of C4H2, C6H2, and Benzene in CRL 618”, Astrophysical Journal Letters, 546 (2): L123—L126, Bibcode:2001ApJ...546L.123C, doi:10.1086/318871
jstor.org
- Faraday, M. (1825). „On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat”. Philosophical Transactions of the Royal Society. 115: 440—466. JSTOR 107752. doi:10.1098/rstl.1825.0022. On pages 443–450, Faraday discusses "bicarburet of hydrogen" (benzene). On pages 449–450, he shows that benzene's empirical formula is C6H6, although he doesn't realize it because he (like most chemists at that time) used the wrong atomic mass for carbon (6 instead of 12).
nih.gov
ncbi.nlm.nih.gov
- Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- Breslow, R.; Guo, T. (1990). „Surface tension measurements show that chaotropic salting-in denaturants are not just water-structure breakers”. Proceedings of the National Academy of Sciences of the United States of America. 87 (1): 167—9. Bibcode:1990PNAS...87..167B. PMC 53221 . PMID 2153285. doi:10.1073/pnas.87.1.167.
nist.gov
webbook.nist.gov
- Benzene in Linstrom, P.J.; Mallard, W.G. (eds.) NIST Chemistry WebBook, NIST Standard Reference Database Number 69. National Institute of Standards and Technology, Gaithersburg MD. http://webbook.nist.gov (retrieved 2014-05-29)
sciencedirect.com
- Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
sigmaaldrich.com
- Sigma-Aldrich Co., Benzene. Приступљено 29. 5. 2014.
wikipedia.org
sr.wikipedia.org
- Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
wiley.com
onlinelibrary.wiley.com
- Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.