メタロール (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "メタロール" in Japanese language version.

refsWebsite
Global rank Japanese rank
2nd place
6th place
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24th place
18th place
107th place
5th place
19th place

doi.org (Global: 2nd place; Japanese: 6th place)

  • Dubac, Jacques; Laporterie, Andre; Manuel, Georges (1990). “Group 14 Metalloles. 1. Synthesis, Organic Chemistry, and Physicochemical Data”. Chemical Reviews 90: 215–263. doi:10.1021/cr00099a008. 
  • Tracy, Henry J.; Mullin, Jerome L.; Klooster, Wim T.; Martin, James A.; Haug, Judith; Wallace, Scott; Rudloe, Isaac; Watts, Kimberly (2005). “Enhanced Photoluminescence from Group 14 Metalloles in Aggregated and Solid Solutions”. Inorganic Chemistry 44 (6): 2003–2011. doi:10.1021/ic049034o. PMID 15762727. 
  • Pelzer, Silke; Wichmann, Karin; Wesendrup, Ralf; Schwerdtfeger, Peter (2002). “Trends in Inversion Barriers IV. The Group 15 Analogous of Pyrrole”. The Journal of Physical Chemistry A 106 (26): 6387. Bibcode2002JPCA..106.6387P. doi:10.1021/jp0203494. 
  • Saito, Masaichi; Nakada, Marisa; Kuwabara, Takuya; Owada, Ryota; Furukawa, Shunsuke; Narayanan, Radhika; Abe, Minori; Hada, Masahiko et al. (2019-08-26). “Inverted Sandwich Rh Complex Bearing a Plumbole Ligand and Its Catalytic Activity”. Organometallics 38 (16): 3099–3103. doi:10.1021/acs.organomet.9b00339. ISSN 0276-7333. https://doi.org/10.1021/acs.organomet.9b00339. 
  • Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario et al. (2021-12-10). “Introduction of plumbole to f-element chemistry” (英語). Chemical Science 13 (4): 945–954. doi:10.1039/D1SC03805B. ISSN 2041-6539. PMC 8790777. PMID 35211259. https://pmc.ncbi.nlm.nih.gov/articles/PMC8790777/. 
  • Atwood, Jerry L.; Hunter, William E.; Alt, Helmut; Rausch, Marvin D. (1976). “The molecular structure of 1,1-bis(.eta.5-cyclopentadienyl)-2,3,4,5-tetraphenyltitanole and its hafnium analogue”. Journal of the American Chemical Society 98 (9): 2454–2459. Bibcode1976JAChS..98.2454A. doi:10.1021/ja00425a012. 
  • Urrego-Riveros, Sara; Ramirez y Medina, Isabel-Maria; Duvinage, Daniel; Lork, Enno; Sönnichsen, Frank D.; Staubitz, Anne (2019). “Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes”. Chemistry – A European Journal 25 (58): 13318–13328. doi:10.1002/chem.201902255. PMC 6851999. PMID 31347203. https://pmc.ncbi.nlm.nih.gov/articles/PMC6851999/. 
  • “Kristallstruktur, 1H-NMR- und Massenspektrum von Tricarbonylferracyclopentadien-tricarbonyleisen, C4H4Fe2(CO)6 [Crystal Structure, Proton NMR and Mass Spectrum of Tricarbonylferracyclopentadienetricarbonyliron, C4H4Fe2(CO)6]”. J. Organomet. Chem. 108 (2): 213–23. (1976). doi:10.1016/S0022-328X(00)82143-9. 

harvard.edu (Global: 18th place; Japanese: 107th place)

ui.adsabs.harvard.edu

  • Pelzer, Silke; Wichmann, Karin; Wesendrup, Ralf; Schwerdtfeger, Peter (2002). “Trends in Inversion Barriers IV. The Group 15 Analogous of Pyrrole”. The Journal of Physical Chemistry A 106 (26): 6387. Bibcode2002JPCA..106.6387P. doi:10.1021/jp0203494. 
  • Atwood, Jerry L.; Hunter, William E.; Alt, Helmut; Rausch, Marvin D. (1976). “The molecular structure of 1,1-bis(.eta.5-cyclopentadienyl)-2,3,4,5-tetraphenyltitanole and its hafnium analogue”. Journal of the American Chemical Society 98 (9): 2454–2459. Bibcode1976JAChS..98.2454A. doi:10.1021/ja00425a012. 

nih.gov (Global: 4th place; Japanese: 24th place)

pubmed.ncbi.nlm.nih.gov

  • Tracy, Henry J.; Mullin, Jerome L.; Klooster, Wim T.; Martin, James A.; Haug, Judith; Wallace, Scott; Rudloe, Isaac; Watts, Kimberly (2005). “Enhanced Photoluminescence from Group 14 Metalloles in Aggregated and Solid Solutions”. Inorganic Chemistry 44 (6): 2003–2011. doi:10.1021/ic049034o. PMID 15762727. 
  • Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario et al. (2021-12-10). “Introduction of plumbole to f-element chemistry” (英語). Chemical Science 13 (4): 945–954. doi:10.1039/D1SC03805B. ISSN 2041-6539. PMC 8790777. PMID 35211259. https://pmc.ncbi.nlm.nih.gov/articles/PMC8790777/. 
  • Urrego-Riveros, Sara; Ramirez y Medina, Isabel-Maria; Duvinage, Daniel; Lork, Enno; Sönnichsen, Frank D.; Staubitz, Anne (2019). “Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes”. Chemistry – A European Journal 25 (58): 13318–13328. doi:10.1002/chem.201902255. PMC 6851999. PMID 31347203. https://pmc.ncbi.nlm.nih.gov/articles/PMC6851999/. 

pmc.ncbi.nlm.nih.gov

worldcat.org (Global: 5th place; Japanese: 19th place)

search.worldcat.org