0000000000008632

AUTHOR

B. Mathiasch

showing 11 related works from this author

Zinn - Chalkogen - Heterocyclen. I. 2.4.6-Hexamethyl-1.3.5-triselena-2.4.6-tristannacyclohexan, Massen- und Schwingungsspektren

2010

The mass spectrum of the title compound exhibits very similar fragmentation patterns compared with the sulfur analogon. The high stability of triply coordinated organotin cations is remarkable. There is no evidence for any stabilisation effects by pπ-dπ bonding concerning the ring bonds. The assignment of the vibration spectra leads to the conclusion that the molecule of triselenastanninane possesses a boat conformation.

CrystallographyFragmentation (mass spectrometry)chemistryStereochemistryCyclohexane conformationMass spectrumMoleculechemistry.chemical_elementGeneral ChemistryVibration spectraSulfurBulletin des Sociétés Chimiques Belges
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ChemInform Abstract: Mixed Group 14-Group 14 Bonds. Part 7. An Incremental System for Estimating 13C NMR Chemical Shifts of Arylated Group 14 Compoun…

2010

Group (periodic table)ChemistryChemical shiftOrganic chemistryMixed groupGeneral MedicineCarbon-13 NMRChemInform
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Zinn - Chalkogen - Heterocyclen. V. 2,2,3,3,5,5,6,6-Octamethyl-1.4-dithia-2,3,5,6-tetpastan-ninan, Darstellung und Zersetzung eines Zinnreichen Heter…

1977

Abstract The title compound can be regarded as a sulfur derivative of the corresponding organoditin compound arid contains -formally- tin in the oxidation state 3. It is prepared in analogy to tris (dimethyltinsulfide).

Inorganic ChemistryTrischemistry.chemical_compoundchemistryOxidation statechemistry.chemical_elementPhysical and Theoretical ChemistryTinSulfurMedicinal chemistryDerivative (chemistry)Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry
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Synthesis and Characterization of the Hybrid Clay-Based Material Montmorillonite-Melanoidin: A Potential Soil Model

2010

The study of the interactions among metals, minerals, and humic substances is essential in understanding the migration of inorganic pollutants in the geosphere. A considerable amount of organic matter in the environment is associated with clay minerals. To understand the role of organic matter in the environment and its association with clay minerals, a hybrid clay-based material (HCM), montmorillonite (STx-1)-melanoidin, was prepared from L-tyrosine and L-glutamic acid by the Maillard reaction. The HCM was characterized by elemental analysis, nuclear magnetic resonance, x-ray photoelectron spectroscopy (XPS), scanning transmission x-ray microscopy (STXM), and thermal analysis. The presence…

chemistry.chemical_classificationMelanoidinSoil Sciencecomplex mixturesSilicatechemistry.chemical_compoundMontmorillonitechemistryX-ray photoelectron spectroscopyChemical engineeringElemental analysisOrganic chemistryOrganic matterThermal analysisClay mineralsSoil Science Society of America Journal
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Carbon-13 NMR parameters of phenyltin halogenides and phenyltin chalcogenides

1981

The 13C NMR shift parameters and couplings to tin are reported for nine phenyltin halogenides and seven phenyltin chalcogenides, as well as the T1 results for Ph2SnTe. A pronounced linear dependence of all coupling constants on the para-carbon shift is discussed.

Coupling constantChemistryPhysical chemistrychemistry.chemical_elementGeneral Materials ScienceGeneral ChemistryCarbon-13 NMRTinOrganic Magnetic Resonance
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CCDC 173863: Experimental Crystal Structure Determination

2002

Related Article: H.Fleischer, B.Mathiasch, D.Schollmeyer|2002|Organometallics|21|526|doi:10.1021/om0104159

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersTrichloro-(2-chloro-3-hydroxypropyl-CO)-tellurium dichloro-(2-chloro-3-oxypropyl-CO)-telluriumExperimental 3D Coordinates
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CCDC 267938: Experimental Crystal Structure Determination

2006

Related Article: H.Fleischer, Y.Dienes, B.Mathiasch, V.Schmitt, D.Schollmeyer|2005|Inorg.Chem.|44|8087|doi:10.1021/ic050814m

Space GroupCrystallographycatena-((mu~2~-(2-aminoethane)thiolato)-((2-aminoethane)thiolato)-cadmium(ii))Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 202462: Experimental Crystal Structure Determination

2006

Related Article: H.Fleischer, Y.Dienes, B.Mathiasch, V.Schmitt, D.Schollmeyer|2005|Inorg.Chem.|44|8087|doi:10.1021/ic050814m

Space GroupCrystallographybis((2-aminoethane)thiolato)-zinc(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 249831: Experimental Crystal Structure Determination

2006

Related Article: H.Fleischer, Y.Dienes, B.Mathiasch, V.Schmitt, D.Schollmeyer|2005|Inorg.Chem.|44|8087|doi:10.1021/ic050814m

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((2-aminoethane)thiolato)-mercury(ii)Experimental 3D Coordinates
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CCDC 207623: Experimental Crystal Structure Determination

2006

Related Article: H.Fleischer, Y.Dienes, B.Mathiasch, V.Schmitt, D.Schollmeyer|2005|Inorg.Chem.|44|8087|doi:10.1021/ic050814m

Space GroupCrystallographyCrystal System2-aminoethanethiolCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 173864: Experimental Crystal Structure Determination

2002

Related Article: H.Fleischer, B.Mathiasch, D.Schollmeyer|2002|Organometallics|21|526|doi:10.1021/om0104159

Trichloro-(2-acetoxy-3-chloropropyl-CO)-telluriumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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