Ferrocén (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ferrocén" in Hungarian language version.

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35doi.org

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1chemicalbook.com

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1nwmissouri.edu

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1sciencelab.com

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1nobelprize.org

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acs.org

pubs.acs.org

Ron Dagani (2002. szeptember 16.). „The Bio Side of Organometallics”. Chemical and Engineering News 80 (37), 23–29. o. DOI:10.1021/cen-v080n037.p023.

archive.org

(1956) „On manganese cyclopentadienide and some chemical reactions of neutral bis-cyclopentadienyl metal compounds”. J. Inorg. Nucl. Chem. 2 (2), 95. o. DOI:10.1016/0022-1902(56)80004-3.
(1990) „A convenient method for the preparation of monolithioferrocene”. Tetrahedron Letters 31 (22), 3121–3124. o. DOI:10.1016/S0040-4039(00)94710-5.

chemicalbook.com

Ferrocene(102-54-5). (Hozzáférés: 2010. február 3.)

doi.org

dx.doi.org

(2004) „Ferrocene: 50 Years of Transition Metal Organometallic Chemistry – From Organic and Inorganic to Supramolecular Chemistry”. ChemInform 35 (43). DOI:10.1002/chin.200443242.
Pauson, P. L. (2001). „Ferrocene-how it all began”. J. Organomet. Chem. 637–639, 637–639. o. DOI:10.1016/S0022-328X(01)01126-3.
(1951) „A New Type of Organo-Iron Compound”. Nature 168 (4285), 1039. o. DOI:10.1038/1681039b0.
Miller, S. A., Tebboth, J. A., Tremaine, J. F. (1952). „114. Dicyclopentadienyliron”. J. Chem. Soc., 632–635. o. DOI:10.1039/JR9520000632.
Pierre Laszlo, Roald Hoffmann, (2000). „Ferrocene: Ironclad History or Rashomon Tale?”. Angewandte Chemie International Edition 39 (1), 123–124. o. DOI:<123::AID-ANIE123>3.0.CO;2-Z 10.1002/(SICI)1521-3773(20000103)39:1<123::AID-ANIE123>3.0.CO;2-Z. PMID 10649350.
(2012) „At Least 60 Years of Ferrocene: The Discovery and Rediscovery of the Sandwich Complexes”. Angew. Chem. Int. Ed 51, 6052–6058. o. DOI:10.1002/anie.201201598.
G. Wilkinson, M. Rosenblum, M. C. Whiting, R. B. Woodward (1952). „The Structure of Iron Bis-Cyclopentadienyl”. Journal of the American Chemical Society 74 (8), 2125–2126. o. DOI:10.1021/ja01128a527.
Dunitz, J. D., Orgel, L. E. (1953). „Bis-Cyclopentadienyl – A Molecular Sandwich”. Nature 171 (4342), 121–122. o. DOI:10.1038/171121a0.
J. Dunitz, L. Orgel, A. Rich (1956). „The crystal structure of ferrocene”. Acta Crystallographica 9 (4), 373–375. o. DOI:10.1107/S0365110X56001091.
P. F. Eiland and R. Pepinsky (1952). „X-ray examination of iron biscyclopentadienyl”. Journal of the American Chemical Society 74 (19), 4971. o. DOI:10.1021/ja01139a527.
(1968) „The Determination of Barriers to Internal Rotation by Means of Electron Diffraction. Ferrocene and Ruthenocene”. Acta Chemica Scandinavica 22, 2653–2670. o. DOI:10.3891/acta.chem.scand.22-2653.
(2006) „The Equilibrium Structure of Ferrocene”. ChemPhysChem 7, 245–249. o. DOI:10.1002/cphc.200500339.
E. W. Abel, N. J. Long, K. G. Orrell, A. G. Osborne, V. Sik (1991). „Dynamic NMR studies of ring rotation in substituted ferrocenes and ruthenocenes”. Journal of Organometallic Chemistry 403, 195–208. o. DOI:10.1016/0022-328X(91)83100-I.
(1951) „A New Type of Organo-Iron Compound”. Nature 168 (4285), 1039. o. DOI:10.1038/1681039b0.
(1954) „{{{title}}}”. J. Am. Chem. Soc. 76 (7), 1970. o. DOI:10.1021/ja01636a080.
(1959) „Cyclopentadienyl and Arene Metal Compounds”. Progress in Inorganic Chemistry 1, 1–124. o. DOI:10.1002/978-0-470-16602-4.ch1.
(1956) „On manganese cyclopentadienide and some chemical reactions of neutral bis-cyclopentadienyl metal compounds”. J. Inorg. Nucl. Chem. 2 (2), 95. o. DOI:10.1016/0022-1902(56)80004-3.
(2006) „New Static Apparatus and Vapor Pressure of Reference Materials: Naphthalene, Benzoic Acid, Benzophenone, and Ferrocene”. Journal of Chemical & Engineering Data 51 (2), 757. o. DOI:10.1021/je050502y.
G.R. Knox, P.L. Pauson and D. Willison (1992). „Ferrocene derivatives. 27. Ferrocenyldimethylphosphine”. Organometallics 11 (8), 2930–2933. o. DOI:10.1021/om00044a038.
G.P. Sollott, H.E. Mertwoy, S. Portnoy and J.L. Snead (1963). „Unsymmetrical Tertiary Phosphines of Ferrocene by Friedel-Crafts Reactions. I. Ferrocenylphenylphosphines”. J. Org. Chem. 28 (4), 1090–1092. o. DOI:10.1021/jo01039a055.
Mark R. St. J. Foreman, Alexandra M. Z. Slawin and J. Derek Woollins (1996). „2,4-Diferrocenyl-1,3-dithiadiphosphetane 2,4-disulfide; structure and reactions with catechols and [PtCl₂(PR₃)₂](R = Et or Bun)”. J. Chem. Soc., Dalton Trans. (18), 3653–3657. o. DOI:10.1039/DT9960003653.
(1990) „A convenient method for the preparation of monolithioferrocene”. Tetrahedron Letters 31 (22), 3121–3124. o. DOI:10.1016/S0040-4039(00)94710-5.
David E. Herbert, Ulrich F. J. Mayer, Ian Manners (2007). „Strained Metallocenophanes and Related Organometallic Rings Containing pi-Hydrocarbon Ligands and Transition-Metal Centers”. Angew. Chem. Int. Ed. 46 (27), 5060–5081. o. DOI:10.1002/anie.200604409.
N. G. Connelly, W. E. Geiger (1996). „Chemical Redox Agents for Organometallic Chemistry”. Chemical Reviews 96 (2), 877–910. o. DOI:10.1021/cr940053x. PMID 11848774.
(1997) „Effective Kinetic Resolution of Secondary Alcohols with a Planar-Chiral Analogue of 4-(dimethylamino)pyridine. Use of the Fe(C₅Ph₅) Group in Asymmetric Catalysis”. J. Am. Chem. Soc. 119 (6), 1492–1493. o. DOI:10.1021/ja963835b.
(2011) „The antimalarial ferroquine: from bench to clinic”. Parasite 18 (3), 207–214. o. DOI:10.1051/parasite/2011183207. ISSN 1252-607X.
S. Top, A. Vessières, G. Leclercq, J. Quivy, J. Tang, J. Vaissermann, M. Huché and G. Jaouen (2003). „Synthesis, Biochemical Properties and Molecular Modelling Studies of Organometallic Specific Estrogen Receptor Modulators (SERMs), the Ferrocifens and Hydroxyferrocifens: Evidence for an Antiproliferative Effect of Hydroxyferrocifens on both Hormone-Dependent and Hormone-Independent Breast Cancer Cell Lines”. Chemistry, a European Journal 9 (21), 5223–36. o. DOI:10.1002/chem.200305024. PMID 14613131.
Ron Dagani (2002. szeptember 16.). „The Bio Side of Organometallics”. Chemical and Engineering News 80 (37), 23–29. o. DOI:10.1021/cen-v080n037.p023.
S. Top, B. Dauer, J. Vaissermann and G. Jaouen (1997). „Facile route to ferrocifen, 1-[4-(2-dimethylaminoethoxy)]-1-(phenyl-2-ferrocenyl-but-1-ene), first organometallic analogue of tamoxifen, by the McMurry reaction”. Journal of Organometallic Chemistry 541, 355–361. o. DOI:10.1016/S0022-328X(97)00086-7.
Devin Conroya, Anna Moisalab, Silvana Cardosoa, Alan Windleb and John Davidson (2010). „Carbon nanotube reactor: Ferrocene decomposition, iron particle growth, nanotube aggregation and scale-up”. Chemical Engineering Science 65 (10), 2965–2977. o. DOI:10.1016/j.ces.2010.01.019.
Liu, Wan-yi; Xu, Qi-hai; Ma, Yong-xiang; Liang, Yong-min; Dong, Ning-li; Guan, De-peng (2001). „Solvent-free synthesis of ferrocenylethene derivatives”. J. Organomet. Chem. 625, 128–132. o. DOI:10.1016/S0022-328X(00)00927-X.
(1990) „An improved photochemical synthesis of azaferrocene”. Journal of Organometallic Chemistry 388, 175. o. DOI:10.1016/0022-328X(90)85359-7.
(1982) „Chemistry of some .eta.5-pyrrolyl- and .eta.1-N-pyrrolyliron complexes”. Inorganic Chemistry 21 (3), 868. o. DOI:10.1021/ic00133a006.
Y. Yu, A.D. Bond, P. W. Leonard, K. P. C. Vollhardt, G. D. Whitener (2006). „Syntheses, Structures, and Reactivity of Radial Oligocyclopentadienyl Metal Complexes: Penta(ferrocenyl)cyclopentadienyl and Congeners”. Angewandte Chemie International Edition 45 (11), 1794–1799. o. DOI:10.1002/anie.200504047. PMID 16470902.
Yong Yu, Andrew D. Bond, Philip W. Leonard, Ulrich J. Lorenz, Tatiana V. Timofeeva, K. Peter C. Vollhardt, Glenn D. Whitener and Andrey A. Yakovenko (2006). „Hexaferrocenylbenzene”. Chem. Commun. (24), 2572–2574. o. DOI:10.1039/b604844g. PMID 16779481.

nih.gov

ncbi.nlm.nih.gov

Pierre Laszlo, Roald Hoffmann, (2000). „Ferrocene: Ironclad History or Rashomon Tale?”. Angewandte Chemie International Edition 39 (1), 123–124. o. DOI:<123::AID-ANIE123>3.0.CO;2-Z 10.1002/(SICI)1521-3773(20000103)39:1<123::AID-ANIE123>3.0.CO;2-Z. PMID 10649350.
N. G. Connelly, W. E. Geiger (1996). „Chemical Redox Agents for Organometallic Chemistry”. Chemical Reviews 96 (2), 877–910. o. DOI:10.1021/cr940053x. PMID 11848774.
S. Top, A. Vessières, G. Leclercq, J. Quivy, J. Tang, J. Vaissermann, M. Huché and G. Jaouen (2003). „Synthesis, Biochemical Properties and Molecular Modelling Studies of Organometallic Specific Estrogen Receptor Modulators (SERMs), the Ferrocifens and Hydroxyferrocifens: Evidence for an Antiproliferative Effect of Hydroxyferrocifens on both Hormone-Dependent and Hormone-Independent Breast Cancer Cell Lines”. Chemistry, a European Journal 9 (21), 5223–36. o. DOI:10.1002/chem.200305024. PMID 14613131.
Y. Yu, A.D. Bond, P. W. Leonard, K. P. C. Vollhardt, G. D. Whitener (2006). „Syntheses, Structures, and Reactivity of Radial Oligocyclopentadienyl Metal Complexes: Penta(ferrocenyl)cyclopentadienyl and Congeners”. Angewandte Chemie International Edition 45 (11), 1794–1799. o. DOI:10.1002/anie.200504047. PMID 16470902.
Yong Yu, Andrew D. Bond, Philip W. Leonard, Ulrich J. Lorenz, Tatiana V. Timofeeva, K. Peter C. Vollhardt, Glenn D. Whitener and Andrey A. Yakovenko (2006). „Hexaferrocenylbenzene”. Chem. Commun. (24), 2572–2574. o. DOI:10.1039/b604844g. PMID 16779481.

nobelprize.org

Press Release: The Nobel Prize in Chemistry 1973. The Royal Swedish Academy of Sciences, 1973

nwmissouri.edu

Material Safety Data Sheet. Ferrocene. MSDS# 03388. Section. https://www.nwmissouri.edu/naturalsciences/sds/f/Ferrocene.pdf . [2021. szeptember 30-i dátummal az eredetiből archiválva]. (Hozzáférés: 2015. december 9.)

orgsyn.org

Geoffrey Wilkinson (1963). „Ferrocene”. Org. Synth.. ; Coll. Vol. 4: 473

osd.org.tr

Application of fuel additives. [2006. május 5-i dátummal az eredetiből archiválva]. (Hozzáférés: 2006. május 5.)

parasite-journal.org

(2011) „The antimalarial ferroquine: from bench to clinic”. Parasite 18 (3), 207–214. o. DOI:10.1051/parasite/2011183207. ISSN 1252-607X.

sciencelab.com

Ferrocene MSDS - ScienceLab. www.sciencelab.com/msds.php?msdsId=992404 . [2015. december 12-i dátummal az eredetiből archiválva]. (Hozzáférés: 2015. december 9.)

web.archive.org

Material Safety Data Sheet. Ferrocene. MSDS# 03388. Section. https://www.nwmissouri.edu/naturalsciences/sds/f/Ferrocene.pdf . [2021. szeptember 30-i dátummal az eredetiből archiválva]. (Hozzáférés: 2015. december 9.)
Ferrocene MSDS - ScienceLab. www.sciencelab.com/msds.php?msdsId=992404 . [2015. december 12-i dátummal az eredetiből archiválva]. (Hozzáférés: 2015. december 9.)
Application of fuel additives. [2006. május 5-i dátummal az eredetiből archiválva]. (Hozzáférés: 2006. május 5.)

worldcat.org

(2011) „The antimalarial ferroquine: from bench to clinic”. Parasite 18 (3), 207–214. o. DOI:10.1051/parasite/2011183207. ISSN 1252-607X.