ビフェニレン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ビフェニレン" in Japanese language version.

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  • “Front Matter”. Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. (2014). p. 209. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4 
  • Waser, Jurg; Lu, Chia-Si (1944). “The Crystal Structure of Biphenylene”. J. Am. Chem. Soc. 66 (12): 2035–2042. doi:10.1021/ja01240a012. 
  • Fawcett, J. K.; Trotter, J. (1966). “A refinement of the structure of biphenylene”. Acta Crystallogr. 20: 87–93. doi:10.1107/s0365110x66000161. 
  • Yokozeki, A.; Wilcox Jr., C. F.; Bauer, S. H. (1974). “Biphenylene. Internuclear distances and their root mean square amplitudes of vibration”. J. Am. Chem. Soc. 96 (4): 1026–1032. doi:10.1021/ja00811a014. 
  • Katritzky, A. R.; Reavill, R. E. (1964). “Nuclear magnetic resonance evidence for partial bond fixation in biphenylene”. Recl. Trav. Chim. Pays-Bas 83 (12): 1230–1232. doi:10.1002/recl.19640831203. 
  • Fraenkel, G.; Asahi, Y.; Mitchell, M. J.; Cava, M. P. (1964). “NMR spectroscopy of benzocyclobutene and biphenylene”. Tetrahedron 20 (5): 1179–1184. doi:10.1016/s0040-4020(01)98985-9. 
  • Dauben Jr., Hyp. J.; Wilson, James D.; Laity, John L. (1969). “Diamagnetic susceptibility exaltation in hydrocarbons”. J. Am. Chem. Soc. 91 (8): 1991–1998. doi:10.1021/ja01036a022. 
  • Anet, F. A. L.; Schenck, G. (1971). “Application of solvent effects to the study of diamagnetic and paramagnetic ring currents”. J. Am. Chem. Soc. 93 (2): 556–557. doi:10.1021/ja00731a061. 
  • Lüder, Johann; de Simone, Monica; Totani, Roberta (2015). “The electronic characterization of biphenylene—Experimental and theoretical insights from core and valence level spectroscopy”. J. Chem. Phys. 142 (7): 074305. Bibcode2015JChPh.142g4305L. doi:10.1063/1.4907723. hdl:11368/2842819. PMID 25702013. https://arts.units.it/bitstream/11368/2842819/1/Lueder_2015.pdf. 
  • Wilcox Jr., Charles F.; Uetrecht, J. P.; Grohman, K. K. (1972). “Cycloocta[def]biphenylene”. J. Am. Chem. Soc. 94 (7): 2532. doi:10.1021/ja00762a068. 
  • Wilcox Jr., Charles F.; Farley, Erik N. (1983). “Dicycloocta[1,2,3,4-def:1',2',3',4'-jkl]biphenylene. Benzenoid Atropism in a Highly Antiaromatic Polycycle”. J. Am. Chem. Soc. 105 (24): 7191–7192. doi:10.1021/ja00362a040. 
  • Wilcox Jr., Charles F.; Farley, Erik N. (1984). “Dicyclooctabiphenylene. Synthesis and Properties”. J. Am. Chem. Soc. 106 (23): 7195–7200. doi:10.1021/ja00335a055. 
  • Wilcox Jr., Charles F.; Farley, Erik N. (1985). “Cyclooctannelated Biphenylenes. Diagnosis of an Anomalous Bond Length by Analysis of Ring Current Geometric Factors”. J. Org. Chem. 50 (3): 351–356. doi:10.1021/jo00203a013. 
  • G. Brunetto, P. A. S. Autreto, L. D. Machado, B. I. Santos, R. P. B. dos Santos, and D. S. Galvao (2012). “Nonzero gap two-dimensional carbon allotrope from porous graphene”. J. Phys. Chem. C 116 (23): 12810–12813. arXiv:1205.6838. Bibcode2012arXiv1205.6838B. doi:10.1021/jp211300n. 
  • Lüder J., Puglia C., Ottosson H., Eriksson O., Sanyal B., Brena B. (2016). “Many-body effects and excitonic features in 2D biphenylene carbon”. J. Chem. Phys. 144 (2): 024702. Bibcode2016JChPh.144b4702L. doi:10.1063/1.4939273. PMID 26772582. 
  • Zhu L., Jin Y.,Xue Q., Li X., Zheng H., Wu T. Ling C. (2016). “Theoretical study of a tunable and strain-controlled nanoporous graphenylene membrane for multifunctional gas separation”. J. Mater. Chem. A 4 (39): 15015–15021. doi:10.1039/C6TA04456E. 
  • Lothrop, W. C. (1941). “Biphenylene”. J. Am. Chem. Soc. 63 (5): 1187–1191. doi:10.1021/ja01850a007. 
  • Campbell, C.D.; Rees, C.W. (1969). “Reactive intermediates. Part I. Synthesis and oxidation of 1- and 2-aminobenzotriazole”. J. Chem. Soc. C 1969 (5): 742–747. doi:10.1039/J39690000742. 

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