Dye regeneration and charge recombination in dye-sensitized solar cells with ferrocene derivatives as redox mediators

Torben Daeneke, Attila J. Mozer, Tae-Hyuk Kwon, Noel W. Duffy, Andrew B. Holmes, Udo Bach and Leone Spiccia

Energy Environ. Sci., 2012, 5, 7090
DOI: 10.1039/c2ee21257a

The molecular structure, equilibrium conformation and barrier to internal rotation in decachloroferrocene, Fe(η-C5Cl5)2, determined by gas electron diffraction

Leo Phillips, Mervyn K. Cooper, Arne Haaland, Svein Samdal, Nina I. Giricheva and Georgiy V. Girichev

Dalton Trans., 2010, 39, 4631
DOI: 10.1039/c001366h

Syntheses and purification of the versatile synthons iodoferrocene and 1,1′-diiodoferrocene

Max Roemer and Christian A. Nijhuis

Dalton Trans., 2014, 43, 11815
DOI: 10.1039/C4DT01787K

The electronic polarizability distribution of several substituted ferrocenes and Di(η6-benzene)chromium

Leonidas Phillips and Gary R. Dennis

J. Chem. Soc., Dalton Trans., 1995, 1469
DOI: 10.1039/DT9950001469

How to get the desired reduction voltage in a single framework! Metallacarborane as an optimal probe for sequential voltage tuning

Màrius Tarrés, Víctor S. Arderiu, Adnana Zaulet, Clara Viñas, Fabrizia Fabrizi de Biani and Francesc Teixidor

Dalton Trans., 2015, 44, 11690
DOI: 10.1039/C5DT01464F

Exploring the boundaries of ferrocenesulfonyl fluoride chemistry

William Erb, Jean-Pierre Hurvois, Yury S. Halauko, Vadim E. Matulis and Thierry Roisnel

Inorg. Chem. Front., 2022, 9, 5862
DOI: 10.1039/D2QI01854C

Mean magnetic susceptibility and its solvent dependence for several substituted ferrocenes, ruthenocene and di(η6-benzene)chromium

Leonidas Phillips

J. Chem. Soc., Dalton Trans., 1994, 3257
DOI: 10.1039/DT9940003257

From ferrocene to 1,2,3,4,5-pentafluoroferrocene: halogen effect on the properties of metallocene

William Erb, Nicolas Richy, Jean-Pierre Hurvois, Paul J. Low and Florence Mongin

Dalton Trans., 2021, 50, 16933
DOI: 10.1039/D1DT03430H

Choosing the right precursor for thermal decomposition solution-phase synthesis of iron nanoparticles: tunable dissociation energies of ferrocene derivatives

Cameron H. W. Kelly and Matthias Lein

Phys. Chem. Chem. Phys., 2016, 18, 32448
DOI: 10.1039/C6CP06921E

Charge-compensatednido-carborane derivatives in the synthesis of iron(ii) bis(dicarbollide) complexes

Marina Yu. Stogniy, Sergey A. Anufriev, Ekaterina V. Bogdanova, Nadezhda A. Gorodetskaya, Alexei A. Anisimov, Kyrill Yu. Suponitsky, Ivan D. Grishin and Igor B. Sivaev

Dalton Trans., 2024, 53, 3363
DOI: 10.1039/D3DT03549B

Redox potential and substituent effects in ferrocene derivatives: II

M.Emília N.P.R.A. Silva, Armando J.L. Pombeiro, João J.R. Fraústo da Silva, Rudolf Herrmann, Norbert Deus and Richard E.Bozak

Journal of Organometallic Chemistry, 1994, 480, 81
DOI: 10.1016/0022-328X(94)87105-1

Synthesis and Characterization of 1,2,3,4,5-Pentafluoroferrocene

Karlheinz Sünkel, Stefan Weigand, Alexander Hoffmann, Sebastian Blomeyer, Christian G. Reuter, Yury V. Vishnevskiy and Norbert W. Mitzel

J. Am. Chem. Soc., 2015, 137, 126
DOI: 10.1021/ja511588p

Preparation and One-Electron Oxidation of Decabromoferrocene

Susanne M. Rupf, Irina S. Dimitrova, Gabriel Schröder and Moritz Malischewski

Organometallics, 2022, 41, 1261
DOI: 10.1021/acs.organomet.2c00157

Outer-Sphere Redox Couples as Shuttles in Dye-Sensitized Solar Cells. Performance Enhancement Based on Photoelectrode Modification via Atomic Layer Deposition

Thomas W. Hamann, Omar K. Farha and Joseph T. Hupp

J. Phys. Chem. C, 2008, 112, 19756
DOI: 10.1021/jp807395g

High-efficiency dye-sensitized solar cells with ferrocene-based electrolytes

Torben Daeneke, Tae-Hyuk Kwon, Andrew B. Holmes, Noel W. Duffy, Udo Bach and Leone Spiccia

Nature Chem, 2011, 3, 211
DOI: 10.1038/nchem.966

Ionization Energy and Reduction Potential in Ferrocene Derivatives: Comparison of Hybrid and Pure DFT Functionals

Mateja Toma, Tea Kuvek and Valerije Vrček

J. Phys. Chem. A, 2020, 124, 8029
DOI: 10.1021/acs.jpca.0c06663

Colorimetric Fluoride Ion Sensing by Polyborylated Ferrocenes: Structural Influences on Thermodynamics and Kinetics

Joanna K. Day, Christopher Bresner, Natalie D. Coombs, Ian A. Fallis, Li-Ling Ooi and Simon Aldridge

Inorg. Chem., 2008, 47, 793
DOI: 10.1021/ic701494p

Coordination chemistry of perhalogenated cyclopentadienes and alkynes. Part 30. New high-yield syntheses of monochloroferrocene and 1,2,3,4,5-pentachloroferrocene. Molecular structures of 1,2-dichloroferrocene and 1,2,3-trichloroferrocene

Stefanie Bernhartzeder and Karlheinz Sünkel

Journal of Organometallic Chemistry, 2012, 716, 146
DOI: 10.1016/j.jorganchem.2012.06.016

Polysubstituted ferrocenes as tunable redox mediators

Sven D Waniek, Jan Klett, Christoph Förster and Katja Heinze

Beilstein J. Org. Chem., 2018, 14, 1004
DOI: 10.3762/bjoc.14.86

1,2,3,4,5-Pentabromoferrocene and related compounds: A simple synthesis of useful precursors

Ian R. Butler

Inorganic Chemistry Communications, 2008, 11, 484
DOI: 10.1016/j.inoche.2008.01.015

Redox-Stable SAMs in Water (pH 0–12) from 1,1′-Biferrocenylene-Terminated Thiols on Gold

Rochus Breuer and Michael Schmittel

Organometallics, 2012, 31, 6642
DOI: 10.1021/om300718k

Redox Shuttle-Based Electrolytes for Dye-Sensitized Solar Cells: Comprehensive Guidance, Recent Progress, and Future Perspective

Masud and Hwan Kyu Kim

ACS Omega, 2023, 8, 6139
DOI: 10.1021/acsomega.2c06843

Synthesis, chemical reactivity and electrochemical behaviour of mono- and difluoro metallocenes

David Bulfield, Marcus Maschke, Max Lieb and Nils Metzler-Nolte

Journal of Organometallic Chemistry, 2015, 797, 125
DOI: 10.1016/j.jorganchem.2015.07.018

Toward Sustainable, Colorless, and Transparent Photovoltaics: State of the Art and Perspectives for the Development of Selective Near‐Infrared Dye‐Sensitized Solar Cells

Fionnuala Grifoni, Matteo Bonomo, Waad Naim, Nadia Barbero, Thomas Alnasser, Iva Dzeba, Marco Giordano, Arshak Tsaturyan, Maxence Urbani, Tomas Torres, Claudia Barolo and Frédéric Sauvage

Advanced Energy Materials, 2021, 11
DOI: 10.1002/aenm.202101598

The Unusual Redox Properties of Fluoroferrocenes Revealed through a Comprehensive Study of the Haloferrocenes

Michael S. Inkpen, Shuoren Du, Mariana Hildebrand, Andrew J. P. White, Nicholas M. Harrison, Tim Albrecht and Nicholas J. Long

Organometallics, 2015, 34, 5461
DOI: 10.1021/acs.organomet.5b00811

1.3 V Inorganic Sequential Redox Chain with an All-Anionic Couple 1–/2– in a Single Framework

Ana B. Buades, Clara Viñas, Xavier Fontrodona and Francesc Teixidor

Inorg. Chem., 2021, 60, 16168
DOI: 10.1021/acs.inorgchem.1c01822