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Serveur d'exploration sur le thulium - Analysis (Allemagne)

Index « Auteurs » - entrée « Igor L. Fedushkin »
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Ian Hewitt < Igor L. Fedushkin < Ines Raabe  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 6.
Ident.Authors (with country if any)Title
000287 (2003) Igor L. Fedushkin [Russie] ; Alexandra A. Skatova ; Vladimir K. Cherkasov ; Valentina A. Chudakova ; Sebastian Dechert ; Markus Hummert ; Herbert Schumann [Allemagne]Reduction of Benzophenone and 9(10H)‐Anthracenone with the Magnesium Complex [(2,6‐iPr2C6H3‐bian)Mg(thf)3]
000333 (2001) Mikhail N. Bochkarev [Russie] ; Igor L. Fedushkin ; Sebastian Dechert ; Anatolii A. Fagin ; Herbert Schumann [Allemagne][NdI2(thf)5], the First Crystallographically Authenticated Neodymium(II) Complex
000344 (2001) Igor L. Fedushkin [Russie] ; Frank Girgsdies ; Herbert Schumann [Allemagne] ; Mikhail N. BochkarevFormation and Structure of Thulium(III) Cyclopentadienides as Products of Reactions Directed Towards the Synthesis of Thulium(II) Cyclopentadienides
000347 (2001) Igor L. Fedushkin [Russie] ; Mikhail N. Bochkarev ; Sebastian Dechert ; Herbert Schumann [Allemagne]A Chemical Definition of the Effective Reducing Power of Thulium(II) Diiodide by Its Reactions with Cyclic Unsaturated Hydrocarbons
000349 (2001) Mikhail N. Bochkarev [Russie] ; Igor L. Fedushkin ; Sebastian Dechert ; Anatolii A. Fagin ; Herbert Schumann [Allemagne][NdI2(thf)5], der erste kristallographisch charakterisierte Neodym(II)‐Komplex
000389 (1999) Herbert Schumann [Allemagne] ; Frank Erbstein ; Dirk F. Karasiak ; Igor L. Fedushkin ; Jörg Demtschuk ; Frank GirgsdiesSynthesis and Characterization of donor‐functionalized ansa‐Cyclopentadienyl‐Indenyl and ansa‐Indenyl‐Indenyl Complexes of Yttrium, Samarium, Thulium, and Lutetium

List of associated KwdEn.i

Nombre de
documents		Descripteur
5Chem
4Hydrogen atoms
4Ligand
4Mmol
4Unit cell
3Bochkarev
3Bond lengths
3Diethyl ether
3Molecular structure
3Molecular structures
3Reaction mixture
3Room temperature
3Schumann
3Solvent molecules
3Thulium
3Verlag gmbh
2Acta crystallogr
2Ambient temperature
2Crude product
2Crystal structures
2Crystallographic data
2Cyclopentadienyl
2Data collection
2Elemental analysis calcd
2Equimolar amounts
2Fedushkin
2Full paper
2Inorg
2Organomet
2Relevant bond lengths
2Space group
2Thermal ellipsoids
2Thulium atom
2Yellow crystals
1Acenaphthylene
1Allg
1Angew
1Anion
1Anorg
1Anthracene
1Aromatic ketones
1Asselt
1Asymmetric unit
1Benzophenone
1Benzophenone ketyl
1Biradical species
1Black crystals
1Bond length
1Calc
1Carbon atoms
1Centroid position
1Centroid positions
1Characteristic ranges
1Chemischen industrie
1Colorless crystals
1Crystal data
1Crystal dimensions
1Cyclic
1Cyclooctatetraene
1Cyclopentadienyl ligands
1Dalton trans
1Deng
1Dianionic ligand
1Diethyl
1Diffraction analysis
1Diiodide
1Dimethylamino group
1Divalent
1Divalent samarium
1Elemental analyses
1Ellipsoid
1Elsevier
1Equivalent atoms
1Ether
1Ether solution
1Excess sodium
1Fagin
1Formula units
1Fudan xuebao
1Full paper formation
1Functionalized side chain
1Green coating
1Hexane
1Homolytic splitting
1Indenyl
1Indenyl ligand
1Indenyl lithium
1Iodine atom
1Isopropyl groups
1Ketyl
1Ketyl radicals
1Lanthanide
1Lanthanide complexes
1Ligation
1Ligation reaction
1Literature methods
1Lithium
1Lithium anthracenide
1Lutetium
1Magnesium

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