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Books on the topic 'Ferrocene'

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Published: 4 June 2021
Last updated: 28 July 2024

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1

Drößmar-Wolf, Marianne. Fe Organoiron Compounds Part A Ferrocene 8. Edited by Adolf Slawisch. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-08850-0.

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2

Phillips, Elisabeth S. Ferrocenes: Compounds, properties, and applications. Hauppauge, N.Y: Nova Science Publisher's, 2011.

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3

Antonio, Togni, and Hayashi Tamio, eds. Ferrocenes: Homogeneous catalysis, organic synthesis, materials science. New York: VCH Publishers, 1994.

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4

D, Rumminger Marc, National Institute of Standards and Technology (U.S.), and Building and Fire Research Laboratory (U.S.), eds. Flame inhibition by ferrocene, carbon dioxide, and trifluoromethane blends: Synergistic and antagonistic effects. Gaithersburg, MD: U.S. Dept. of Commerce, Technology Administration, National Institute of Standards and Technology, 1999.

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5

Wang, Li, and Haojie Yu. Synthesis, Properties and Applications of Ferrocene-based Derivatives, Polymers and Hydrogels. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6062-5.

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6

E, Westphal T., and United States. Bureau of Mines., eds. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C. (810 7th St., N.W., MS#9800, Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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7

Zeller, H. William. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C: United States Dept. of the Interior, Bureau of Mines, 1992.

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8

E, Westphal T., and United States. Bureau of Mines, eds. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C. (810 7th St., N.W., MS#9800, Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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9

Zeller, H. William. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C. (810 7th St., N.W., MS#9800, Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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10

E, Westphal T., and United States. Bureau of Mines., eds. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C. (810 7th St., N.W., MS#9800, Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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11

Zeller, H. William. Effectiveness of iron-based fuel additives on diesel soot control. Washington, D.C. (810 7th St., N.W., MS#9800, Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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12

S, Abd-El-Aziz Alaa, ed. Organoiron polymers. Hoboken, N.J: Wiley-Interscience, 2004.

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13

tpnika, PETR, ed. Ferrocenes. Chichester, UK: John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/9780470985663.

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14

Dai, Li-Xin, and Xue-Long Hou, eds. Chiral Ferrocenes in Asymmetric Catalysis. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2009. http://dx.doi.org/10.1002/9783527628841.

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15

Petr, Štěpnička, ed. Ferrocenes: Ligands, materials and biomolecules. Chichester, England: J.Wiley, 2008.

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16

Xue-Long, Hou, ed. Chiral ferrocenes in asymmetric catalysis. Weinheim: Wiley-VCH, 2010.

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17

Jaworska-Augustyniak, Anna. Fotochemiczne własności elektrono-donorowo-akceptorowych kompleksów ferrocenu, kobaltocenu i niklocenu. Poznań: Wydawn. Nauk. Uniwersytetu im. Adama Mickiewicza w Poznaniu, 1988.

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18

Purser, Alexander Simon. Novel organo-palladium complexes containing 1,1[superior ,]- substituted ferrocenyl diphosphine ligands. Birmingham: University of Birmingham, 1998.

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19

ößmar-Wolf, Marianne, Adolf Slawisch, R. Bohrer, U. Nohl, and H. J. Richter-Ditten. Fe Organoiron Compounds: Ferrocene 10. Springer London, Limited, 2013.

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20

Rudolph, E., Adolf Slawisch, R. Bohrer, U. Nohl, H. J. Richter-Ditten, and Marianne Drößmar-Wolf. Fe Organoiron Compounds: Ferrocene 10. Springer, 2013.

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21

Michaile, Sherie. Kinetic study of the formation of hydrogen gas from the reaction of [1.1] ferrocenophanes with strong acids. 1985.

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22

Stepnicka, Petr. Ferrocenes. Wiley & Sons, Incorporated, John, 2008.

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23

Löffler, Uwe. Monosubstituierte Ferrocene als Mediatoren in amperometrischen Biosensoren. 1991.

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24

Togni, Antonio, and Tamio Hayashi. Ferrocenes: Homogeneous Catalysis, Organic Synthesis, Materials Science. Wiley & Sons, Limited, John, 2007.

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25

Togni, Antonio, and Tamio Hayashi. Ferrocenes: Homogeneous Catalysis, Organic Synthesis, Materials Science. Wiley & Sons, Incorporated, John, 2008.

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26

Massey, Jason. Self-assembly of block copolymers containing poly(ferrocene). Dept of Chemistry, U of Toronto, 2000.

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27

Togni, Antonio. Ferrocenes: Homogeneous Catalysis/Organic Synthesis/Materials Science. Wiley-VCH Verlag GmbH, 1995.

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28

Togni, Antonio. Ferrocenes: Homogeneous Catalysis, Organic Synthesis, Materials Science. Vch Pub, 1994.

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29

Resendes, Rui. Ring-opened poly(ferrocene)s: New directions and applications. 2000.

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30

Ferrocene an Unprecedented Organometallic - Applications in Various Fields [Working Title]. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.78519.

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31

Elihn, Karine. Synthesis of Carbon-Covered Iron Nanoparticles by Photolysis of Ferrocene. Uppsala Universitet, 2002.

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32

Kasper, Markus. Ferrocene, carbon particles, and PAH in a methane diffusion flame. 1998.

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33

Hobi, Markus Josef. Ferrocene als Donoren in Charge-Transfer-Komplexen: Synthese und Charakterisierung. 1997.

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34

Barfuss, Susanne. Massenspektroskopische Untersuchung substituierter Ferrocene nach Anregung mit Elektronen und Photonen. 1989.

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35

Wang, Li, and Haojie Yu. Synthesis, Properties and Applications of Ferrocene-based Derivatives, Polymers and Hydrogels. Springer, 2018.

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36

Grant, J. Ferrocene containing smoke suppressants and flame retardants for semi rigid polyvinyl chloride. 1993.

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37

Abd-El-Aziz, Alaa S., E. Jr Carraher Charles, U. Jr Pittman Charles, John E. Sheats, and Martel Zeldin. Macromolecules Containing Metal and Metal-Like Elements, Organoiron Polymers (Macromolecules Containing Metal and Metal-like Elements). Wiley-Interscience, 2003.

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38

Slawisch, Adolf, Edgar Rudolph, and Marianne Drössmar-Wolf. Fe Organoiron Compounds: Mononuclear Disubstituted Ferrocene Derivatives with C-, H-, and O-Containing Substituents. Springer, 1986.

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39

össmar-Wolf, Marianne. Fe Organoiron Compounds: Mononuclear Disubstituted Ferrocene Derivatives with C-, H-, and o-Containing Substituents. Springer London, Limited, 2013.

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40

Faust, J]rgen, Wolfgang Petz, and Christa Siebert. Nzungsband A-C Fe-Organische Verbindungen / Organoiron Compounds Teil B Einkernige Verbindungen (Ohne Ferrocene) / Mononuclear C. Springer, 1988.

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41

Togni, A., and T. Hayashi, eds. Ferrocenes. Wiley, 1994. http://dx.doi.org/10.1002/9783527615599.

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42

Eland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.

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Abstract:
In the vast majority of conjugated and aromatic molecules, the outermost occupied orbitals are either of π‎ character or non-bonding lone pairs belonging to heteroatoms. These are the orbitals from which double ionisation gives rise to most of the distinct bands that can be discerned in their spectra. Double photoionisation spectra of ethylene, butadiene, pyrrole, furan, thiophene, benzene, hexafluorobenzene, toluene, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, azulene, quinoline, biphenyl, TDME, iron pentacarbonyl, ferrocene, and TMPPD are presented with analysis where possible. The effects of inner valence Auger effects are also emphasised, which can greatly increase the intensity of double photoionisation. In this chapter, the molecules are ordered mainly in the usual way by number of atoms, then by molecular weight, but the authors have put closely related molecules together where possible.
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43

Stepnicka, Petr. Ferrocenes: Ligands, Materials and Biomolecules. Wiley & Sons, Limited, John, 2008.

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44

Stepnicka, Petr. Ferrocenes: Ligands, Materials and Biomolecules. Wiley & Sons, Incorporated, John, 2008.

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45

Agada, Otokpa Christopher-Marius. Catalytic efficiency of zerovalent iron compounds as paint driers compared with conventional substances: The use of ferrocene and other iron compounds as driers in autoxidative paint systems at ambient and elevated temperatures. Bradford, 1985.

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46

Dai, Li-Xin, and Xue-Long Hou. Chiral Ferrocenes in Asymmetric Catalysis: Synthesis and Applications. Wiley & Sons, Incorporated, John, 2010.

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47

Dai, Li-Xin, and Xue-Long Hou. Chiral Ferrocenes in Asymmetric Catalysis: Synthesis and Applications. Wiley & Sons, Limited, John, 2010.

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48

Birenheide, Bernhard. Neuartige Mono- und Multimetallische Komplexe Auf Basis des Ferrocens. Logos Verlag Berlin, 2022.

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49

Mark, James E., Harry R. Allcock, and Robert West. Inorganic Polymers. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195131192.001.0001.

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Polymer chemistry and technology form one of the major areas of molecular and materials science. This field impinges on nearly every aspect of modern life, from electronics technology, to medicine, to the wide range of fibers, films, elastomers, and structural materials on which everyone depends. Although most of these polymers are organic materials, attention is being focused increasingly toward polymers that contain inorganic elements as well as organic components. The goal of Inorganic Polymers is to provide a broad overview of inorganic polymers in a way that will be useful to both the uninitiated and those already working in this field. There are numerous reasons for being interested in inorganic polymers. One is the simple need to know how structure affects the properties of a polymer, particularly outside the well-plowed area of organic materials. Another is the bridge that inorganic polymers provide between polymer science and ceramics. More and more chemistry is being used in the preparation of ceramics of carefully controlled structure, and inorganic polymers are increasingly important precursor materials in such approaches. This new edition begins with a brief introductory chapter. That is followed with a discussion of the characteristics and characterization of polymers, with examples taken from the field. Other chapters in the book detail the synthesis, reaction chemistry, molecular structure, and uses of polyphosphazenes, polysiloxanes, and polysilanes. The coverage in the second edition has been updated and expanded significantly to cover advances and interesting trends since the first edition appeared. Three new chapters have been added, focusing on ferrocene-based polymers, other phosphorous-containing polymers, and boron-containing polymers; inorganic-organic hybrid composites; and preceramic inorganic polymers.
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50

Baumann, Markus Peter. Asymmetrische Heck-Reaktionen mit chiralen P,N-Ferrocenyl-Liganden. 2000.

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