Ferrocene (English Wikipedia)

International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1041. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
Fulem, Michal; Růžička, Květoslav; Červinka, Ctirad; Rocha, Marisa A.A.; Santos, Luís M.N.B.F.; Berg, Robert F. (February 2013). "Recommended vapor pressure and thermophysical data for ferrocene" (pdf). The Journal of Chemical Thermodynamics. 57: 530–540. doi:10.1016/j.jct.2012.07.023. Retrieved 15 January 2026.
Werner H (June 2012). "At least 60 years of ferrocene: the discovery and rediscovery of the sandwich complexes". Angewandte Chemie. 51 (25): 6052–6058. Bibcode:2012ACIE...51.6052W. doi:10.1002/anie.201201598. PMID 22573490.
Pauson PL (2001). "Ferrocene—how it all began". Journal of Organometallic Chemistry. 637–639: 3–6. doi:10.1016/S0022-328X(01)01126-3.
Miller SA, Tebboth JA, Tremaine JF (1952). "114. Dicyclopentadienyliron". J. Chem. Soc.: 632–635. doi:10.1039/JR9520000632.
Laszlo P, Hoffmann R (January 2000). "Ferrocene: Ironclad History or Rashomon Tale?". Angewandte Chemie. 39 (1): 123–124. doi:10.1002/(SICI)1521-3773(20000103)39:1<123::AID-ANIE123>3.0.CO;2-Z. PMID 10649350.
Kealy TJ, Pauson PL (1951). "A New Type of Organo-Iron Compound". Nature. 168 (4285): 1039–1040. Bibcode:1951Natur.168.1039K. doi:10.1038/1681039b0. S2CID 4181383.
Wilkinson G, Rosenblum M, Whiting MC, Woodward RB (1952-03-24). "The structure of iron bis-cyclopentadienyl". J. Am. Chem. Soc. 74 (8): 2125–2126. Bibcode:1952JAChS..74.2125W. doi:10.1021/ja01128a527.
Woodward, R. B.; Rosenblum, M.; Whiting, M. C. (1952-06-02). "A New Aromatic System". Journal of the American Chemical Society. 74 (13): 3458–3459. Bibcode:1952JAChS..74.3458W. doi:10.1021/ja01133a543. ISSN 0002-7863.
Fischer EO, Pfab W (1952). "Zur Kristallstruktur der Di-Cyclopentadienyl-Verbindungen des zweiwertigen Eisens, Kobalts und Nickels" [On the crystal structure of the bis-cyclopentadienyl compounds of divalent iron, cobalt and nickel]. Zeitschrift für Naturforschung B. 7 (7): 377–379. doi:10.1515/znb-1952-0701.
Okuda J (2016-12-28). "Ferrocene - 65 Years After". European Journal of Inorganic Chemistry. 2017 (2): 217–219. doi:10.1002/ejic.201601323. ISSN 1434-1948.
Eiland PF, Pepinsky R (1952). "X-ray Examination of Iron Biscyclopentadienyl". J. Am. Chem. Soc. 74 (19): 4971. Bibcode:1952JAChS..74.4971E. doi:10.1021/ja01139a527.
Dunitz JD, Orgel LE (1953). "Bis-Cyclopentadienyl – A Molecular Sandwich". Nature. 171 (4342): 121–122. Bibcode:1953Natur.171..121D. doi:10.1038/171121a0. S2CID 4263761.
Dunitz JD, Orgel L, Rich A (1956). "The crystal structure of ferrocene". Acta Crystallogr. 9 (4): 373–375. Bibcode:1956AcCry...9..373D. doi:10.1107/S0365110X56001091.
Mingos DM (2001). "A Historical Perspective on Dewar's Landmark Contribution to Organometallic Chemistry". J. Organomet. Chem. 635 (1–2): 1–8. doi:10.1016/S0022-328X(01)01155-X.
Abel EW, Long NJ, Orrell KG, Osborne AG, Šik V (1991). "Dynamic NMR studies of ring rotation in substituted ferrocenes and ruthenocenes". J. Org. Chem. 403 (1–2): 195–208. doi:10.1016/0022-328X(91)83100-I.
Seiler P, Dunitz JD (1982). "Low-temperature crystallization of orthorhombic ferrocene: structure analysis at 98 K". Acta Crystallographica Section B. 38 (6): 1741–1745. Bibcode:1982AcCrB..38.1741S. doi:10.1107/s0567740882007080. ISSN 0567-7408.
Haaland A, Nilsson JE (1968). "The Determination of Barriers to Internal Rotation by Means of Electron Diffraction. Ferrocene and Ruthenocene". Acta Chem. Scand. 22: 2653–2670. doi:10.3891/acta.chem.scand.22-2653 (inactive 26 July 2025).{{cite journal}}: CS1 maint: DOI inactive as of July 2025 (link)
Coriani S, Haaland A, Helgaker T, Jørgensen P (January 2006). "The equilibrium structure of ferrocene". ChemPhysChem. 7 (1): 245–249. doi:10.1002/cphc.200500339. PMID 16404766.
Katrusiak, Andrzej; Rusek, Michalina; Dušek, Michal; Petříček, Václav; Szafrański, Marek (2023-04-06). "Dipole-Moment Modulation in New Incommensurate Ferrocene". The Journal of Physical Chemistry Letters. 14 (13): 3111–3119. doi:10.1021/acs.jpclett.3c00215. ISSN 1948-7185. PMC 10084461. PMID 36951481.
Wang, Feng; Mohammadi, Narges; Best, Stephen P.; Appadoo, Dominique; Chantler, Christopher T. (2021). "Dominance of eclipsed ferrocene conformer in solutions revealed by the IR spectra between 400 and 500 cm-1". Radiation Physics and Chemistry. 188 109590. Bibcode:2021RaPC..18809590W. doi:10.1016/j.radphyschem.2021.109590.
Wilkinson G, Pauson PL, Cotton FA (1954). "Bis-cyclopentadienyl Compounds of Nickel and Cobalt". J. Am. Chem. Soc. 76 (7): 1970–1974. Bibcode:1954JAChS..76.1970W. doi:10.1021/ja01636a080.
Wilkinson G, Cotton FA. "Cyclopentadienyl and Arene Metal Compounds". Progress in Inorganic Chemistry. Vol. 1. pp. 1–124. doi:10.1002/9780470166024.ch1. ISBN 978-0-470-16602-4.
Wilkinson G (1956). "Ferrocene". Organic Syntheses. 36: 31. doi:10.15227/orgsyn.036.0031.
Wilkinson G, Cotton FA, Birmingham JM (1956). "On manganese cyclopentadienide and some chemical reactions of neutral bis-cyclopentadienyl metal compounds". J. Inorg. Nucl. Chem. 2 (2): 95–113. doi:10.1016/0022-1902(56)80004-3.
Bozak RE (1966). "Acetylation of Ferrocene: A Chromatography Experiment for Elementary Organic Laboratory". J. Chem. Educ. 43 (2): 73. Bibcode:1966JChEd..43...73B. doi:10.1021/ed043p73.
Knox GR, Pauson PL, Willison D (1992). "Ferrocene derivatives. 27. Ferrocenyldimethylphosphine". Organometallics. 11 (8): 2930–2933. doi:10.1021/om00044a038.
Sollott GP, Mertwoy HE, Portnoy S, Snead JL (1963). "Unsymmetrical Tertiary Phosphines of Ferrocene by Friedel–Crafts Reactions. I. Ferrocenylphenylphosphines". J. Org. Chem. 28 (4): 1090–1092. doi:10.1021/jo01039a055.
Rausch, M. D. (1963). "Metallocene Chemistry—A Decade of Progress". Canadian Journal of Chemistry. 41 (5): 1289–1314. Bibcode:1963CaJCh..41.1289R. doi:10.1139/v63-182.
St J Foreman MR, Alexandra MZ, Slawin AM, Woollins JD (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. doi:10.1039/DT9960003653.
Malischewski M, Seppelt K, Sutter J, Heinemann FW, Dittrich B, Meyer K (October 2017). "Protonation of Ferrocene: A Low-Temperature X-ray Diffraction Study of [Cp₂ FeH](PF₆ ) Reveals an Iron-Bound Hydrido Ligand". Angewandte Chemie. 56 (43): 13372–13376. doi:10.1002/anie.201704854. PMID 28834022.
Busacca, Carl A.; Eriksson, Magnus C.; Haddad, Nizar; Han, Z. Steve; Lorenz, Jon C.; Qu, Bo; Zeng, Xingzhong; Senanayake, Chris H. (2013). "Practical Synthesis of Di-tert-Butyl-Phosphinoferrocene". Organic Syntheses. 90: 316. doi:10.15227/orgsyn.090.0316.
Togni, A.; Hayashi, T., eds. (1994). Ferrocenes. doi:10.1002/9783527615599. ISBN 978-3-527-29048-2.
Cardona CM, Li W, Kaifer AE, Stockdale D, Bazan GC (May 2011). "Electrochemical considerations for determining absolute frontier orbital energy levels of conjugated polymers for solar cell applications". Advanced Materials. 23 (20): 2367–2371. Bibcode:2011AdM....23.2367C. doi:10.1002/adma.201004554. PMID 21462372. S2CID 40766788.
Pavlishchuk, Vitaly V; Addison, Anthony W (January 2000). "Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25°C". Inorganica Chimica Acta. 298 (1): 97–102. doi:10.1016/S0020-1693(99)00407-7.
Mygind JB, Deissler NH, Li S, Fu X, Kibsgaard J, Chorkendorff I (1 March 2025). "Hydrogen Oxidation Beyond Water: In Search of Proton Mediation Pathways". ACS Electrochemistry. X (X). American Chemical Society: X–X. doi:10.1021/acselectrochem.5c00009.
Connelly NG, Geiger WE (March 1996). "Chemical Redox Agents for Organometallic Chemistry". Chemical Reviews. 96 (2): 877–910. doi:10.1021/cr940053x. PMID 11848774.
Sirbu D, Turta C, Gibson EA, Benniston AC (September 2015). "The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(II) and copper(II) complexes". Dalton Transactions. 44 (33): 14646–14655. doi:10.1039/C5DT02191J. PMID 26213204.
Lennox AJ, Nutting JE, Stahl SS (January 2018). "Selective electrochemical generation of benzylic radicals enabled by ferrocene-based electron-transfer mediators". Chemical Science. 9 (2): 356–361. doi:10.1039/C7SC04032F. PMC 5909123. PMID 29732109.
Dannenberg JJ, Richards JH (1965-04-01). "Photosensitization by Ferrocene. Photochemistry of Higher Electronic Excited States". Journal of the American Chemical Society. 87 (7): 1626–1627. Bibcode:1965JAChS..87.1626D. doi:10.1021/ja01085a048. ISSN 0002-7863.
Sirbu D, Turta C, Benniston AC, Abou-Chahine F, Lemmetyinen H, Tkachenko NV, et al. (2014-05-23). "Synthesis and properties of a meso- tris–ferrocene appended zinc(II) porphyrin and a critical evaluation of its dye sensitised solar cell (DSSC) performance". RSC Advances. 4 (43): 22733–22742. Bibcode:2014RSCAd...422733S. doi:10.1039/C4RA03105A. ISSN 2046-2069.
Malischewski M, Adelhardt M, Sutter J, Meyer K, Seppelt K (August 2016). "Isolation and structural and electronic characterization of salts of the decamethylferrocene dication". Science. 353 (6300): 678–682. Bibcode:2016Sci...353..678M. doi:10.1126/science.aaf6362. PMID 27516596. S2CID 43385610.
Ruble JC, Latham HA, Fu GC (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. doi:10.1021/ja963835b.
Atkinson RC, Gibson VC, Long NJ (June 2004). "The syntheses and catalytic applications of unsymmetrical ferrocene ligands". Chemical Society Reviews. 33 (5): 313–328. doi:10.1039/B316819K. PMID 15272371.
Blaser HU (2002). "Solvias Josiphos ligands: From discovery to technical applications". Topics in Catalysis. 19: 3–16. doi:10.1023/a:1013832630565. S2CID 95738043.
van Staveren DR, Metzler-Nolte N (December 2004). "Bioorganometallic chemistry of ferrocene". Chemical Reviews. 104 (12): 5931–5985. doi:10.1021/cr0101510. PMID 15584693.
Ong YC, Gasser G (December 2020). "Organometallic compounds in drug discovery: Past, present and future" (PDF). Drug Discovery Today: Technologies. 37: 117–124. doi:10.1016/j.ddtec.2019.06.001. PMID 34895650. S2CID 198268304.
Biot C, Nosten F, Fraisse L, Ter-Minassian D, Khalife J, Dive D (August 2011). "The antimalarial ferroquine: from bench to clinic". Parasite. 18 (3): 207–214. doi:10.1051/parasite/2011183207. PMC 3671469. PMID 21894260.
Roux C, Biot C (April 2012). "Ferrocene-based antimalarials". Future Medicinal Chemistry. 4 (6): 783–797. doi:10.4155/fmc.12.26. PMID 22530641.
Wani WA, Jameel E, Baig U, Mumtazuddin S, Hun LT (August 2015). "Ferroquine and its derivatives: new generation of antimalarial agents". European Journal of Medicinal Chemistry. 101: 534–551. doi:10.1016/j.ejmech.2015.07.009. PMC 7115395. PMID 26188909.
Adoke Y, Zoleko-Manego R, Ouoba S, Tiono AB, Kaguthi G, Bonzela JE, et al. (May 2021). "A randomized, double-blind, phase 2b study to investigate the efficacy, safety, tolerability and pharmacokinetics of a single-dose regimen of ferroquine with artefenomel in adults and children with uncomplicated Plasmodium falciparum malaria". Malaria Journal. 20 (1) 222. doi:10.1186/s12936-021-03749-4. PMC 8135182. PMID 34011358.
Gu H, Mu S, Qiu G, Liu X, Zhang L, Yuan Y, Astruc D (June 2018). "Redox-stimuli-responsive drug delivery systems with supramolecular ferrocenyl-containing polymers for controlled release". Coordination Chemistry Reviews. 364: 51–85. doi:10.1016/j.ccr.2018.03.013. ISSN 0010-8545. S2CID 103022297.
Ornelas C (2011). "Application of ferrocene and its derivatives in cancer research". New Journal of Chemistry. 35 (10): 1973. doi:10.1039/c1nj20172g. S2CID 56521492.
Babin VN, Belousov YA, Borisov VI, Gumenyuk VV, Nekrasov YS, Ostrovskaya LA, et al. (2014). "Ferrocenes as potential anticancer drugs. Facts and hypotheses". Russ. Chem. Bull. 63 (11): 2405–2422. doi:10.1007/s11172-014-0756-7. S2CID 94618726.
Top S, Vessières A, Leclercq G, Quivy J, Tang J, Vaissermann J, et al. (November 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): 5223–5236. doi:10.1002/chem.200305024. PMID 14613131.
Zakrzewski J, Giannotti C (1990). "An improved photochemical synthesis of azaferrocene". J. Organomet. Chem. 388 (1–2): 175–179. doi:10.1016/0022-328X(90)85359-7.
Efraty A, Jubran N, Goldman A (1982). "Chemistry of some η⁵-pyrrolyl- and η¹-N-pyrrolyliron complexes". Inorg. Chem. 21 (3): 868–873. doi:10.1021/ic00133a006.
Abdul-Rahman, S.; Houlton, A.; Roberts, R. M. G.; Silver, J. (1989) [27 May 1988]. "A spectroscopic study of bis(η⁶-arene)iron(II) salts". Journal of Organometallic Chemistry. 359 (3). Netherlands: Elsevier Seqouia: 333. doi:10.1016/0022-328x(89)88096-9.
Yu Y, Bond AD, Leonard PW, Vollhardt KP, Whitener GD (March 2006). "Syntheses, structures, and reactivity of radial oligocyclopentadienyl metal complexes: penta(ferrocenyl)cyclopentadienyl and congeners". Angewandte Chemie. 45 (11): 1794–1799. Bibcode:2006ACIE...45.1794Y. doi:10.1002/anie.200504047. PMID 16470902.
Yu Y, Bond AD, Leonard PW, Lorenz UJ, Timofeeva TV, Vollhardt KP, et al. (June 2006). "Hexaferrocenylbenzene". Chemical Communications (24): 2572–2574. doi:10.1039/b604844g. PMID 16779481.
Pietschnig R (October 2016). "Polymers with pendant ferrocenes". Chemical Society Reviews. 45 (19): 5216–5231. doi:10.1039/C6CS00196C. PMID 27156979.
Conroy D, Moisala A, Cardoso S, Windle A, Davidson J (2010). "Carbon nanotube reactor: Ferrocene decomposition, iron particle growth, nanotube aggregation and scale-up". Chem. Eng. Sci. 65 (10): 2965–2977. doi:10.1016/j.ces.2010.01.019.
Elbert J, Gallei M, Rüttiger C, Brunsen A, Didzoleit H, Stühn B, Rehahn M (2013). "Ferrocene Polymers for Switchable Surface Wettability". Organometallics. 32 (20): 5873–5878. doi:10.1021/om400468p.

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Werner H (June 2012). "At least 60 years of ferrocene: the discovery and rediscovery of the sandwich complexes". Angewandte Chemie. 51 (25): 6052–6058. Bibcode:2012ACIE...51.6052W. doi:10.1002/anie.201201598. PMID 22573490.
Kealy TJ, Pauson PL (1951). "A New Type of Organo-Iron Compound". Nature. 168 (4285): 1039–1040. Bibcode:1951Natur.168.1039K. doi:10.1038/1681039b0. S2CID 4181383.
Wilkinson G, Rosenblum M, Whiting MC, Woodward RB (1952-03-24). "The structure of iron bis-cyclopentadienyl". J. Am. Chem. Soc. 74 (8): 2125–2126. Bibcode:1952JAChS..74.2125W. doi:10.1021/ja01128a527.
Woodward, R. B.; Rosenblum, M.; Whiting, M. C. (1952-06-02). "A New Aromatic System". Journal of the American Chemical Society. 74 (13): 3458–3459. Bibcode:1952JAChS..74.3458W. doi:10.1021/ja01133a543. ISSN 0002-7863.
Eiland PF, Pepinsky R (1952). "X-ray Examination of Iron Biscyclopentadienyl". J. Am. Chem. Soc. 74 (19): 4971. Bibcode:1952JAChS..74.4971E. doi:10.1021/ja01139a527.
Dunitz JD, Orgel LE (1953). "Bis-Cyclopentadienyl – A Molecular Sandwich". Nature. 171 (4342): 121–122. Bibcode:1953Natur.171..121D. doi:10.1038/171121a0. S2CID 4263761.
Dunitz JD, Orgel L, Rich A (1956). "The crystal structure of ferrocene". Acta Crystallogr. 9 (4): 373–375. Bibcode:1956AcCry...9..373D. doi:10.1107/S0365110X56001091.
Seiler P, Dunitz JD (1982). "Low-temperature crystallization of orthorhombic ferrocene: structure analysis at 98 K". Acta Crystallographica Section B. 38 (6): 1741–1745. Bibcode:1982AcCrB..38.1741S. doi:10.1107/s0567740882007080. ISSN 0567-7408.
Wang, Feng; Mohammadi, Narges; Best, Stephen P.; Appadoo, Dominique; Chantler, Christopher T. (2021). "Dominance of eclipsed ferrocene conformer in solutions revealed by the IR spectra between 400 and 500 cm-1". Radiation Physics and Chemistry. 188 109590. Bibcode:2021RaPC..18809590W. doi:10.1016/j.radphyschem.2021.109590.
Wilkinson G, Pauson PL, Cotton FA (1954). "Bis-cyclopentadienyl Compounds of Nickel and Cobalt". J. Am. Chem. Soc. 76 (7): 1970–1974. Bibcode:1954JAChS..76.1970W. doi:10.1021/ja01636a080.
Bozak RE (1966). "Acetylation of Ferrocene: A Chromatography Experiment for Elementary Organic Laboratory". J. Chem. Educ. 43 (2): 73. Bibcode:1966JChEd..43...73B. doi:10.1021/ed043p73.
Rausch, M. D. (1963). "Metallocene Chemistry—A Decade of Progress". Canadian Journal of Chemistry. 41 (5): 1289–1314. Bibcode:1963CaJCh..41.1289R. doi:10.1139/v63-182.
Cardona CM, Li W, Kaifer AE, Stockdale D, Bazan GC (May 2011). "Electrochemical considerations for determining absolute frontier orbital energy levels of conjugated polymers for solar cell applications". Advanced Materials. 23 (20): 2367–2371. Bibcode:2011AdM....23.2367C. doi:10.1002/adma.201004554. PMID 21462372. S2CID 40766788.
Dannenberg JJ, Richards JH (1965-04-01). "Photosensitization by Ferrocene. Photochemistry of Higher Electronic Excited States". Journal of the American Chemical Society. 87 (7): 1626–1627. Bibcode:1965JAChS..87.1626D. doi:10.1021/ja01085a048. ISSN 0002-7863.
Sirbu D, Turta C, Benniston AC, Abou-Chahine F, Lemmetyinen H, Tkachenko NV, et al. (2014-05-23). "Synthesis and properties of a meso- tris–ferrocene appended zinc(II) porphyrin and a critical evaluation of its dye sensitised solar cell (DSSC) performance". RSC Advances. 4 (43): 22733–22742. Bibcode:2014RSCAd...422733S. doi:10.1039/C4RA03105A. ISSN 2046-2069.
Malischewski M, Adelhardt M, Sutter J, Meyer K, Seppelt K (August 2016). "Isolation and structural and electronic characterization of salts of the decamethylferrocene dication". Science. 353 (6300): 678–682. Bibcode:2016Sci...353..678M. doi:10.1126/science.aaf6362. PMID 27516596. S2CID 43385610.
Yu Y, Bond AD, Leonard PW, Vollhardt KP, Whitener GD (March 2006). "Syntheses, structures, and reactivity of radial oligocyclopentadienyl metal complexes: penta(ferrocenyl)cyclopentadienyl and congeners". Angewandte Chemie. 45 (11): 1794–1799. Bibcode:2006ACIE...45.1794Y. doi:10.1002/anie.200504047. PMID 16470902.

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Sirbu D, Turta C, Gibson EA, Benniston AC (September 2015). "The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(II) and copper(II) complexes". Dalton Transactions. 44 (33): 14646–14655. doi:10.1039/C5DT02191J. PMID 26213204.

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Werner H (June 2012). "At least 60 years of ferrocene: the discovery and rediscovery of the sandwich complexes". Angewandte Chemie. 51 (25): 6052–6058. Bibcode:2012ACIE...51.6052W. doi:10.1002/anie.201201598. PMID 22573490.
Laszlo P, Hoffmann R (January 2000). "Ferrocene: Ironclad History or Rashomon Tale?". Angewandte Chemie. 39 (1): 123–124. doi:10.1002/(SICI)1521-3773(20000103)39:1<123::AID-ANIE123>3.0.CO;2-Z. PMID 10649350.
Coriani S, Haaland A, Helgaker T, Jørgensen P (January 2006). "The equilibrium structure of ferrocene". ChemPhysChem. 7 (1): 245–249. doi:10.1002/cphc.200500339. PMID 16404766.
Katrusiak, Andrzej; Rusek, Michalina; Dušek, Michal; Petříček, Václav; Szafrański, Marek (2023-04-06). "Dipole-Moment Modulation in New Incommensurate Ferrocene". The Journal of Physical Chemistry Letters. 14 (13): 3111–3119. doi:10.1021/acs.jpclett.3c00215. ISSN 1948-7185. PMC 10084461. PMID 36951481.
Malischewski M, Seppelt K, Sutter J, Heinemann FW, Dittrich B, Meyer K (October 2017). "Protonation of Ferrocene: A Low-Temperature X-ray Diffraction Study of [Cp₂ FeH](PF₆ ) Reveals an Iron-Bound Hydrido Ligand". Angewandte Chemie. 56 (43): 13372–13376. doi:10.1002/anie.201704854. PMID 28834022.
Cardona CM, Li W, Kaifer AE, Stockdale D, Bazan GC (May 2011). "Electrochemical considerations for determining absolute frontier orbital energy levels of conjugated polymers for solar cell applications". Advanced Materials. 23 (20): 2367–2371. Bibcode:2011AdM....23.2367C. doi:10.1002/adma.201004554. PMID 21462372. S2CID 40766788.
Connelly NG, Geiger WE (March 1996). "Chemical Redox Agents for Organometallic Chemistry". Chemical Reviews. 96 (2): 877–910. doi:10.1021/cr940053x. PMID 11848774.
Sirbu D, Turta C, Gibson EA, Benniston AC (September 2015). "The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(II) and copper(II) complexes". Dalton Transactions. 44 (33): 14646–14655. doi:10.1039/C5DT02191J. PMID 26213204.
Lennox AJ, Nutting JE, Stahl SS (January 2018). "Selective electrochemical generation of benzylic radicals enabled by ferrocene-based electron-transfer mediators". Chemical Science. 9 (2): 356–361. doi:10.1039/C7SC04032F. PMC 5909123. PMID 29732109.
Malischewski M, Adelhardt M, Sutter J, Meyer K, Seppelt K (August 2016). "Isolation and structural and electronic characterization of salts of the decamethylferrocene dication". Science. 353 (6300): 678–682. Bibcode:2016Sci...353..678M. doi:10.1126/science.aaf6362. PMID 27516596. S2CID 43385610.
Atkinson RC, Gibson VC, Long NJ (June 2004). "The syntheses and catalytic applications of unsymmetrical ferrocene ligands". Chemical Society Reviews. 33 (5): 313–328. doi:10.1039/B316819K. PMID 15272371.
van Staveren DR, Metzler-Nolte N (December 2004). "Bioorganometallic chemistry of ferrocene". Chemical Reviews. 104 (12): 5931–5985. doi:10.1021/cr0101510. PMID 15584693.
Ong YC, Gasser G (December 2020). "Organometallic compounds in drug discovery: Past, present and future" (PDF). Drug Discovery Today: Technologies. 37: 117–124. doi:10.1016/j.ddtec.2019.06.001. PMID 34895650. S2CID 198268304.
Biot C, Nosten F, Fraisse L, Ter-Minassian D, Khalife J, Dive D (August 2011). "The antimalarial ferroquine: from bench to clinic". Parasite. 18 (3): 207–214. doi:10.1051/parasite/2011183207. PMC 3671469. PMID 21894260.
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Ferrocene (English Wikipedia)

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