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Korrannulen (Uzbek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Korrannulen" in Uzbek language version.

refsWebsite
Global rank Uzbek rank
40doi.org
2nd place
3rd place
26nih.gov
4th place
7th place
5harvard.edu
18th place
35th place
1uva.nl
3,518th place
low place
1arxiv.org
69th place
186th place
1worldcat.org
5th place
10th place

arxiv.org

  • Wong, B. M. (2009). „Noncovalent interactions in supramolecular complexes: a study on corannulene and the double concave buckycatcher“. Journal of Computational Chemistry. 30-jild, № 1. 51–56-bet. arXiv:1004.4243. doi:10.1002/jcc.21022. PMID 18504779.

doi.org

  • Scott, L. T.; Bronstein, H. E.; Preda, D. V.; Ansems, R. B. M.; Bratcher, M. S.; Hagen, S. (1999). „Geodesic polyarenes with exposed concave surfaces“. Pure and Applied Chemistry. 71-jild, № 2. 209-bet. doi:10.1351/pac199971020209.
  • Scott, L. T.; Hashemi, M. M.; Bratcher, M. S. (1992). „Corannulene bowl-to-bowl inversion is rapid at room temperature“. Journal of the American Chemical Society. 114-jild, № 5. 1920–1921-bet. doi:10.1021/ja00031a079.
  • Barth, W. E.; Lawton, R. G. (1966). „Dibenzo[ghi,mno]fluoranthene“. Journal of the American Chemical Society. 88-jild, № 2. 380–381-bet. doi:10.1021/ja00954a049.
  • Lawton, Richard G.; Barth, Wayne E. (April 1971). „Synthesis of corannulene“. Journal of the American Chemical Society. 93-jild, № 7. 1730–1745-bet. doi:10.1021/ja00736a028.
  • Scott, L. T.; Hashemi, M. M.; Meyer, D. T.; Warren, H. B. (1991). „Corannulene. A convenient new synthesis“. Journal of the American Chemical Society. 113-jild, № 18. 7082–7084-bet. doi:10.1021/ja00018a082.
  • Sygula, A.; Rabideau, P. W. (2000). „A Practical, Large Scale Synthesis of the Corannulene System“. Journal of the American Chemical Society. 122-jild, № 26. 6323–6324-bet. doi:10.1021/ja0011461.
  • Butterfield, A.; Gilomen, B.; Siegel, J. (2012). „Kilogram-Scale Production of Corannulene“. Organic Process Research & Development. 16-jild, № 4. 664–676-bet. doi:10.1021/op200387s.
  • Wu, Y.; Bandera, D.; Maag, R.; Linden, A.; Baldridge, K.; Siegel, J. (2008). „Multiethynyl corannulenes: synthesis, structure, and properties“. Journal of the American Chemical Society. 130-jild, № 32. 10729–10739-bet. doi:10.1021/ja802334n. PMID 18642812.
  • Mack, J.; Vogel, P.; Jones, D.; Kaval, N.; Sutton, A. (2007). „The development of corannulene-based blue emitters“. Organic & Biomolecular Chemistry. 5-jild, № 15. 2448–2452-bet. doi:10.1039/b705621d. PMID 17637965. Manba xatosi: Invalid <ref> tag; name "Mack" defined multiple times with different content
  • Gershoni-Poranne, R.; Pappo, D.; Solel, E.; Keinan, E. (2009). „Corannulene ethers via Ullmann condensation“. Organic Letters. 11-jild, № 22. 5146–5149-bet. doi:10.1021/ol902352k. PMID 19905024.
  • Baldridge, K.; Hardcastle, K.; Seiders, T.; Siegel, J. (2010). „Synthesis, structure and properties of decakis(phenylthio)corannulene“. Organic & Biomolecular Chemistry. 8-jild, № 1. 53–55-bet. doi:10.1039/b919616a. PMID 20024131.
  • Choi, H.; Kim, C.; Park, K. M.; Kim, J.; Kang, Y.; Ko, J. (2009). „Synthesis and structure of penta-platinum σ-bonded derivatives of corannulene“. Journal of Organometallic Chemistry. 694-jild, № 22. 3529–3532-bet. doi:10.1016/j.jorganchem.2009.07.015.
  • Pappo, D.; Mejuch, T.; Reany, O.; Solel, E.; Gurram, M.; Keinan, E. (2009). „Diverse Functionalization of Corannulene: Easy Access to Pentagonal Superstructure“. Organic Letters. 11-jild, № 5. 1063–1066-bet. doi:10.1021/ol8028127. PMID 19193048. Manba xatosi: Invalid <ref> tag; name "pappo" defined multiple times with different content
  • Nishida, S.; Morita, Y.; Ueda, A.; Kobayashi, T.; Fukui, K.; Ogasawara, K.; Sato, K.; Takui, T.; Nakasuji, K. (2008). „Curve-structured phenalenyl chemistry: synthesis, electronic structure, and bowl-inversion barrier of a phenalenyl-fused corannulene anion“. Journal of the American Chemical Society. 130-jild, № 45. 14954–14955-bet. doi:10.1021/ja806708j. PMID 18937470.
  • Steinberg, B.; Jackson, E.; Filatov, A.; Wakamiya, A.; Petrukhina, M.; Scott, L. (2009). „Aromatic pi-systems more curved than C(60). The complete family of all indenocorannulenes synthesized by iterative microwave-assisted intramolecular arylations“. Journal of the American Chemical Society. 131-jild, № 30. 10537–10545-bet. doi:10.1021/ja9031852. PMID 19722628.
  • Topolinski, Berit; Schmidt, Bernd M.; Kathan, Michael; Troyanov, Sergej I.; Lentz, Dieter (2012). „Corannulenylferrocenes: towards a 1D, non-covalent metal–organic nanowire“. Chem. Commun. 48-jild, № 50. 6298–6300-bet. doi:10.1039/C2CC32275G. PMID 22595996.
  • Sygula, A.; Rabideau, P. W. (1995). „Structure and inversion barriers of corannulene, its dianion and tetraanion. An ab initio study“. Journal of Molecular Structure: THEOCHEM. 333-jild, № 3. 215–226-bet. doi:10.1016/0166-1280(94)03961-J.
  • Monaco, G.; Scott, L.; Zanasi, R. (2008). „Magnetic euripi in corannulene“. The Journal of Physical Chemistry A. 112-jild, № 35. 8136–8147-bet. Bibcode:2008JPCA..112.8136M. doi:10.1021/jp8038779. PMID 18693706.
  • Ayalon, A.; Sygula, A.; Cheng, P.; Rabinovitz, M.; Rabideau, P.; Scott, L. (1994). „Stable High-Order Molecular Sandwiches: Hydrocarbon Polyanion Pairs with Multiple Lithium Ions Inside and out“. Science. 265-jild, № 5175. 1065–1067-bet. Bibcode:1994Sci...265.1065A. doi:10.1126/science.265.5175.1065. PMID 17832895.
  • Aprahamian, I.; Eisenberg, D.; Hoffman, R.; Sternfeld, T.; Matsuo, Y.; Jackson, E.; Nakamura, E.; Scott, L.; Sheradsky, T. (2005). „Ball-and-socket stacking of supercharged geodesic polyarenes: bonding by interstitial lithium ions“. Journal of the American Chemical Society. 127-jild, № 26. 9581–9587-bet. doi:10.1021/ja0515102. PMID 15984885.
  • Zabula, A. V. (2011). „A Main Group Metal Sandwich: Five Lithium Cations Jammed Between Two Corannulene Tetraanion Decks“. Science. 333-jild, № 6045. 1008–1011-bet. Bibcode:2011Sci...333.1008Z. doi:10.1126/science.1208686. PMID 21852497.
  • Aprahamian, I.; Preda, D.; Bancu, M.; Belanger, A.; Sheradsky, T.; Scott, L.; Rabinovitz, M. (2006). „Reduction of bowl-shaped hydrocarbons: dianions and tetraanions of annelated corannulenes“. The Journal of Organic Chemistry. 71-jild, № 1. 290–298-bet. doi:10.1021/jo051949c. PMID 16388648.
  • Spisak, S. N.; Zabula, A. V.; Filatov, A. S.; Rogachev, A. Y.; Petrukhina, M. A. (2011). „Selective Endo and Exo Binding of Alkali Metals to Corannulene“. Angewandte Chemie International Edition. 50-jild, № 35. 8090–8094-bet. doi:10.1002/anie.201103028. PMID 21748832.
  • Galué, Héctor Alvaro; Rice, Corey A.; Steill, Jeffrey D.; Oomens, Jos (1-yanvar 2011-yil). „Infrared spectroscopy of ionized corannulene in the gas phase“ (PDF). The Journal of Chemical Physics. 134-jild, № 5. 054310-bet. Bibcode:2011JChPh.134e4310G. doi:10.1063/1.3540661. PMID 21303123.{{cite magazine}}: CS1 maint: date format ()
  • Zabula, A. V.; Spisak, S. N.; Filatov, A. S.; Rogachev, A. Y.; Petrukhina, M. A. (2011). „A Strain-Releasing Trap for Highly Reactive Electrophiles: Structural Characterization of Bowl-Shaped Arenium Carbocations“. Angewandte Chemie International Edition. 50-jild, № 13. 2971–2974-bet. doi:10.1002/anie.201007762. PMID 21404379.
  • Eisenberg, D.; Filatov, A.; Jackson, E.; Rabinovitz, M.; Petrukhina, M.; Scott, L.; Shenhar, R. (2008). „Bicorannulenyl: stereochemistry of a C40H18 biaryl composed of two chiral bowls“. The Journal of Organic Chemistry. 73-jild, № 16. 6073–6078-bet. doi:10.1021/jo800359z. PMID 18505292.
  • Eisenberg, D.; Quimby, J. M.; Jackson, E. A.; Scott, L. T.; Shenhar, R. (2010). „The Bicorannulenyl Dianion: A Charged Overcrowded Ethylene“. Angewandte Chemie International Edition. 49-jild, № 41. 7538–7542-bet. doi:10.1002/anie.201002515. PMID 20814993.
  • Eisenberg, D.; Quimby, J. M.; Jackson, E. A.; Scott, L. T.; Shenhar, R. (2010). „Highly Charged Supramolecular Oligomers Based on the Dimerization of Corannulene Tetraanion“. Chemical Communications. 46-jild, № 47. 9010–9012-bet. doi:10.1039/c0cc03965a. PMID 21057679.
  • Sygula, A.; Fronczek, F.; Sygula, R.; Rabideau, P.; Olmstead, M. (2007). „A double concave hydrocarbon buckycatcher“. Journal of the American Chemical Society. 129-jild, № 13. 3842–3843-bet. doi:10.1021/ja070616p. PMID 17348661.
  • Wong, B. M. (2009). „Noncovalent interactions in supramolecular complexes: a study on corannulene and the double concave buckycatcher“. Journal of Computational Chemistry. 30-jild, № 1. 51–56-bet. arXiv:1004.4243. doi:10.1002/jcc.21022. PMID 18504779.
  • Kobryn, L.; Henry, W. P.; Fronczek, F. R.; Sygula, R.; Sygula, A. (2009). „Molecular clips and tweezers with corannulene pincers“. Tetrahedron Letters. 50-jild, № 51. 7124–7127-bet. doi:10.1016/j.tetlet.2009.09.177.
  • Miyajima, D.; Tashiro, K.; Araoka, F.; Takezoe, H.; Kim, J.; Kato, K.; Takata, M.; Aida, T. (2009). „Liquid crystalline corannulene responsive to electric field“. Journal of the American Chemical Society. 131-jild, № 1. 44–45-bet. doi:10.1021/ja808396b. PMID 19128171.
  • Seiders, T. Jon; Baldridge, Kim K.; O'Connor, Joseph M.; Siegel, Jay S. (1997). „Hexahapto Metal Coordination to Curved Polyaromatic Hydrocarbon Surfaces: The First Transition Metal Corannulene Complex“. J. Am. Chem. Soc. 119-jild, № 20. 4781–4782-bet. doi:10.1021/ja964380t.
  • Siegel, Jay S.; Baldridge, Kim K.; Linden, Anthony; Dorta, Reto (2006). „d8 Rhodium and Iridium Complexes of Corannulene“. J. Am. Chem. Soc. 128-jild, № 33. 10644–10645-bet. doi:10.1021/ja062110x. PMID 16910635.
  • Petrukhina, M. A. (2008). „Coordination of buckybowls: the first concave-bound metal complex“. Angewandte Chemie International Edition in English. 47-jild, № 9. 1550–1552-bet. doi:10.1002/anie.200704783. PMID 18214869.
  • Zhu, B.; Ellern, A.; Sygula, A.; Sygula, R.; Angelici, R. J. (2007). „η6-Coordination of the Curved Carbon Surface of Corannulene (C20H10) to (η6-arene)M2+(M = Ru, Os)“. Organometallics. 26-jild, № 7. 1721–1728-bet. doi:10.1021/om0610795.
  • Petrukhina, M. A.; Sevryugina, Y.; Rogachev, A. Y.; Jackson, E. A.; Scott, L. T. (2006). „Corannulene: A Preference forexo-Metal Binding. X-ray Structural Characterization of [Ru2(O2CCF3)2(CO)4·(η2-C20H10)2]“. Organometallics. 25-jild, № 22. 5492–5495-bet. doi:10.1021/om060350f.
  • Siegel, J.; Baldridge, K.; Linden, A.; Dorta, R. (2006). „D8 rhodium and iridium complexes of corannulene“. Journal of the American Chemical Society. 128-jild, № 33. 10644–10645-bet. doi:10.1021/ja062110x. PMID 16910635.
  • Bandera, D.; Baldridge, K. K.; Linden, A.; Dorta, R.; Siegel, J. S. (2011). „Stereoselective Coordination of C5-Symmetric Corannulene Derivatives with an Enantiomerically Pure [RhI(nbd*)] Metal Complex“. Angewandte Chemie International Edition. 50-jild, № 4. 865–867-bet. doi:10.1002/anie.201006877. PMID 21246679.
  • Diana, Nooramalina; Yamada, Yasuhiro; Gohda, Syun; Ono, Hironobu; Kubo, Shingo; Sato, Satoshi (2021-02-01). „Carbon materials with high pentagon density“. Journal of Materials Science (inglizcha). 56-jild, № 4. 2912–2943-bet. Bibcode:2021JMatS..56.2912D. doi:10.1007/s10853-020-05392-x. ISSN 1573-4803.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wu, Y.; Bandera, D.; Maag, R.; Linden, A.; Baldridge, K.; Siegel, J. (2008). „Multiethynyl corannulenes: synthesis, structure, and properties“. Journal of the American Chemical Society. 130-jild, № 32. 10729–10739-bet. doi:10.1021/ja802334n. PMID 18642812.
  • Mack, J.; Vogel, P.; Jones, D.; Kaval, N.; Sutton, A. (2007). „The development of corannulene-based blue emitters“. Organic & Biomolecular Chemistry. 5-jild, № 15. 2448–2452-bet. doi:10.1039/b705621d. PMID 17637965. Manba xatosi: Invalid <ref> tag; name "Mack" defined multiple times with different content
  • Gershoni-Poranne, R.; Pappo, D.; Solel, E.; Keinan, E. (2009). „Corannulene ethers via Ullmann condensation“. Organic Letters. 11-jild, № 22. 5146–5149-bet. doi:10.1021/ol902352k. PMID 19905024.
  • Baldridge, K.; Hardcastle, K.; Seiders, T.; Siegel, J. (2010). „Synthesis, structure and properties of decakis(phenylthio)corannulene“. Organic & Biomolecular Chemistry. 8-jild, № 1. 53–55-bet. doi:10.1039/b919616a. PMID 20024131.
  • Pappo, D.; Mejuch, T.; Reany, O.; Solel, E.; Gurram, M.; Keinan, E. (2009). „Diverse Functionalization of Corannulene: Easy Access to Pentagonal Superstructure“. Organic Letters. 11-jild, № 5. 1063–1066-bet. doi:10.1021/ol8028127. PMID 19193048. Manba xatosi: Invalid <ref> tag; name "pappo" defined multiple times with different content
  • Nishida, S.; Morita, Y.; Ueda, A.; Kobayashi, T.; Fukui, K.; Ogasawara, K.; Sato, K.; Takui, T.; Nakasuji, K. (2008). „Curve-structured phenalenyl chemistry: synthesis, electronic structure, and bowl-inversion barrier of a phenalenyl-fused corannulene anion“. Journal of the American Chemical Society. 130-jild, № 45. 14954–14955-bet. doi:10.1021/ja806708j. PMID 18937470.
  • Steinberg, B.; Jackson, E.; Filatov, A.; Wakamiya, A.; Petrukhina, M.; Scott, L. (2009). „Aromatic pi-systems more curved than C(60). The complete family of all indenocorannulenes synthesized by iterative microwave-assisted intramolecular arylations“. Journal of the American Chemical Society. 131-jild, № 30. 10537–10545-bet. doi:10.1021/ja9031852. PMID 19722628.
  • Topolinski, Berit; Schmidt, Bernd M.; Kathan, Michael; Troyanov, Sergej I.; Lentz, Dieter (2012). „Corannulenylferrocenes: towards a 1D, non-covalent metal–organic nanowire“. Chem. Commun. 48-jild, № 50. 6298–6300-bet. doi:10.1039/C2CC32275G. PMID 22595996.
  • Monaco, G.; Scott, L.; Zanasi, R. (2008). „Magnetic euripi in corannulene“. The Journal of Physical Chemistry A. 112-jild, № 35. 8136–8147-bet. Bibcode:2008JPCA..112.8136M. doi:10.1021/jp8038779. PMID 18693706.
  • Ayalon, A.; Sygula, A.; Cheng, P.; Rabinovitz, M.; Rabideau, P.; Scott, L. (1994). „Stable High-Order Molecular Sandwiches: Hydrocarbon Polyanion Pairs with Multiple Lithium Ions Inside and out“. Science. 265-jild, № 5175. 1065–1067-bet. Bibcode:1994Sci...265.1065A. doi:10.1126/science.265.5175.1065. PMID 17832895.
  • Aprahamian, I.; Eisenberg, D.; Hoffman, R.; Sternfeld, T.; Matsuo, Y.; Jackson, E.; Nakamura, E.; Scott, L.; Sheradsky, T. (2005). „Ball-and-socket stacking of supercharged geodesic polyarenes: bonding by interstitial lithium ions“. Journal of the American Chemical Society. 127-jild, № 26. 9581–9587-bet. doi:10.1021/ja0515102. PMID 15984885.
  • Zabula, A. V. (2011). „A Main Group Metal Sandwich: Five Lithium Cations Jammed Between Two Corannulene Tetraanion Decks“. Science. 333-jild, № 6045. 1008–1011-bet. Bibcode:2011Sci...333.1008Z. doi:10.1126/science.1208686. PMID 21852497.
  • Aprahamian, I.; Preda, D.; Bancu, M.; Belanger, A.; Sheradsky, T.; Scott, L.; Rabinovitz, M. (2006). „Reduction of bowl-shaped hydrocarbons: dianions and tetraanions of annelated corannulenes“. The Journal of Organic Chemistry. 71-jild, № 1. 290–298-bet. doi:10.1021/jo051949c. PMID 16388648.
  • Spisak, S. N.; Zabula, A. V.; Filatov, A. S.; Rogachev, A. Y.; Petrukhina, M. A. (2011). „Selective Endo and Exo Binding of Alkali Metals to Corannulene“. Angewandte Chemie International Edition. 50-jild, № 35. 8090–8094-bet. doi:10.1002/anie.201103028. PMID 21748832.
  • Galué, Héctor Alvaro; Rice, Corey A.; Steill, Jeffrey D.; Oomens, Jos (1-yanvar 2011-yil). „Infrared spectroscopy of ionized corannulene in the gas phase“ (PDF). The Journal of Chemical Physics. 134-jild, № 5. 054310-bet. Bibcode:2011JChPh.134e4310G. doi:10.1063/1.3540661. PMID 21303123.{{cite magazine}}: CS1 maint: date format ()
  • Zabula, A. V.; Spisak, S. N.; Filatov, A. S.; Rogachev, A. Y.; Petrukhina, M. A. (2011). „A Strain-Releasing Trap for Highly Reactive Electrophiles: Structural Characterization of Bowl-Shaped Arenium Carbocations“. Angewandte Chemie International Edition. 50-jild, № 13. 2971–2974-bet. doi:10.1002/anie.201007762. PMID 21404379.
  • Eisenberg, D.; Filatov, A.; Jackson, E.; Rabinovitz, M.; Petrukhina, M.; Scott, L.; Shenhar, R. (2008). „Bicorannulenyl: stereochemistry of a C40H18 biaryl composed of two chiral bowls“. The Journal of Organic Chemistry. 73-jild, № 16. 6073–6078-bet. doi:10.1021/jo800359z. PMID 18505292.
  • Eisenberg, D.; Quimby, J. M.; Jackson, E. A.; Scott, L. T.; Shenhar, R. (2010). „The Bicorannulenyl Dianion: A Charged Overcrowded Ethylene“. Angewandte Chemie International Edition. 49-jild, № 41. 7538–7542-bet. doi:10.1002/anie.201002515. PMID 20814993.
  • Eisenberg, D.; Quimby, J. M.; Jackson, E. A.; Scott, L. T.; Shenhar, R. (2010). „Highly Charged Supramolecular Oligomers Based on the Dimerization of Corannulene Tetraanion“. Chemical Communications. 46-jild, № 47. 9010–9012-bet. doi:10.1039/c0cc03965a. PMID 21057679.
  • Sygula, A.; Fronczek, F.; Sygula, R.; Rabideau, P.; Olmstead, M. (2007). „A double concave hydrocarbon buckycatcher“. Journal of the American Chemical Society. 129-jild, № 13. 3842–3843-bet. doi:10.1021/ja070616p. PMID 17348661.
  • Wong, B. M. (2009). „Noncovalent interactions in supramolecular complexes: a study on corannulene and the double concave buckycatcher“. Journal of Computational Chemistry. 30-jild, № 1. 51–56-bet. arXiv:1004.4243. doi:10.1002/jcc.21022. PMID 18504779.
  • Miyajima, D.; Tashiro, K.; Araoka, F.; Takezoe, H.; Kim, J.; Kato, K.; Takata, M.; Aida, T. (2009). „Liquid crystalline corannulene responsive to electric field“. Journal of the American Chemical Society. 131-jild, № 1. 44–45-bet. doi:10.1021/ja808396b. PMID 19128171.
  • Siegel, Jay S.; Baldridge, Kim K.; Linden, Anthony; Dorta, Reto (2006). „d8 Rhodium and Iridium Complexes of Corannulene“. J. Am. Chem. Soc. 128-jild, № 33. 10644–10645-bet. doi:10.1021/ja062110x. PMID 16910635.
  • Petrukhina, M. A. (2008). „Coordination of buckybowls: the first concave-bound metal complex“. Angewandte Chemie International Edition in English. 47-jild, № 9. 1550–1552-bet. doi:10.1002/anie.200704783. PMID 18214869.
  • Siegel, J.; Baldridge, K.; Linden, A.; Dorta, R. (2006). „D8 rhodium and iridium complexes of corannulene“. Journal of the American Chemical Society. 128-jild, № 33. 10644–10645-bet. doi:10.1021/ja062110x. PMID 16910635.
  • Bandera, D.; Baldridge, K. K.; Linden, A.; Dorta, R.; Siegel, J. S. (2011). „Stereoselective Coordination of C5-Symmetric Corannulene Derivatives with an Enantiomerically Pure [RhI(nbd*)] Metal Complex“. Angewandte Chemie International Edition. 50-jild, № 4. 865–867-bet. doi:10.1002/anie.201006877. PMID 21246679.

uva.nl

pure.uva.nl

worldcat.org