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非配位性アニオン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "非配位性アニオン" in Japanese language version.

refsWebsite
Global rank Japanese rank
10doi.org
2nd place
6th place
6nih.gov
4th place
24th place
1escholarship.org
1,523rd place
3,636th place
1harvard.edu
18th place
107th place

doi.org

  • I. Krossing & I. Raabe (2004). “Noncoordinating Anions - Fact or Fiction? A Survey of Likely Candidates”. Angewandte Chemie International Edition 43 (16): 2066–2090. doi:10.1002/anie.200300620. PMID 15083452. 
  • Honeychuck, R. V.; Hersh, W. H. (1989). “Coordination of "Noncoordinating" Anions: Synthesis, Characterization, and X-ray Crystal Structures of Fluorine-Bridged [SbF6]−, [BF4]−, and [PF6]− Adducts of [R3P(CO)3(NO)W]+. An Unconventional Order of Anion Donor Strength”. Inorganic Chemistry 28 (14): 2869–2886. doi:10.1021/ic00313a034. 
  • Mayfield, H. G.; Bull, W. E. (1971). “Co-ordinating Tendencies of the Hexafluorophosphate Ion”. J. Chem. Soc. A (14): 2279–2281. doi:10.1039/J19710002279. 
  • Santiso-Quiñones, Gustavo; Reisinger, Andreas; Slattery, John; Krossing, Ingo (2007). “Homoleptic Cu–phosphorus and Cu–ethene complexes”. Chemical Communications (47): 5046. doi:10.1039/b710899k. 
  • N. A. Yakelis; R. G. Bergman (2005). “Sodium Tetrakis(3,5-trifluoromethyl)phenylborate (NaBArF24): Safe Preparation, Standardized Purification, and Analysis of Hydration”. Organometallics 24 (14): 3579–3581. doi:10.1021/om0501428. PMC 2600718. PMID 19079785. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600718/. 
  • M. Brookhart; B. Grant; A. F. Volpe, Jr. (1992). “[(3,5-(CF3)2C6H3)4B]-[H(OEt2)2]+: a convenient reagent for generation and stabilization of cationic, highly electrophilic organometallic complexes”. Organometallics 11 (11): 3920–3922. doi:10.1021/om00059a071. 
  • H. Nishida; N. Takada; M. Yoshimura; T. Sonods; H. Kobayashi (1984). “Tetrakis(3,5-bis(trifluoromethyl)phenyl)borate. Highly lipophilic stable anionic agent for solvent-extraction of cations”. Bulletin of the Chemical Society of Japan 57 (9): 2600. doi:10.1246/bcsj.57.2600. 
  • Jutzi, P.; Müller, C.; Stammler, A.; Stammler, H. G. (2000). “Synthesis, Crystal Structure, and Application of the Oxonium Acid [H(OEt2)2]+[B(C6F5)4]−”. Organometallics 19 (7): 1442. doi:10.1021/om990612w. 
  • G.Erker (2005). “Tris(pentafluorophenyl)borane: a Special Boron Lewis Acid for Special Reactions”. Dalton Transactions (11): 1883–1890. doi:10.1039/b503688g. PMID 15909033. 
  • Kim, K.-C.; Reed, C. A.; Elliott, D. W.; Mueller, L. J.; Tham, F.; Lin, L.; Lambert, J. B. (2002). “Crystallographic Evidence for a Free Silylium Ion”. Science 297 (5582): 825–827. Bibcode: 2002Sci...297..825K. doi:10.1126/science.1073540. PMID 12161650. http://www.escholarship.org/uc/item/88j06088. 

escholarship.org

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • I. Krossing & I. Raabe (2004). “Noncoordinating Anions - Fact or Fiction? A Survey of Likely Candidates”. Angewandte Chemie International Edition 43 (16): 2066–2090. doi:10.1002/anie.200300620. PMID 15083452. 
  • N. A. Yakelis; R. G. Bergman (2005). “Sodium Tetrakis(3,5-trifluoromethyl)phenylborate (NaBArF24): Safe Preparation, Standardized Purification, and Analysis of Hydration”. Organometallics 24 (14): 3579–3581. doi:10.1021/om0501428. PMC 2600718. PMID 19079785. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600718/. 
  • G.Erker (2005). “Tris(pentafluorophenyl)borane: a Special Boron Lewis Acid for Special Reactions”. Dalton Transactions (11): 1883–1890. doi:10.1039/b503688g. PMID 15909033. 
  • Kim, K.-C.; Reed, C. A.; Elliott, D. W.; Mueller, L. J.; Tham, F.; Lin, L.; Lambert, J. B. (2002). “Crystallographic Evidence for a Free Silylium Ion”. Science 297 (5582): 825–827. Bibcode: 2002Sci...297..825K. doi:10.1126/science.1073540. PMID 12161650. http://www.escholarship.org/uc/item/88j06088. 

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov