0000000001302144

AUTHOR

Rolfe H. Herber

showing 23 related works from this author

Dispersion Forces and Counterintuitive Steric Effects in Main Group Molecules: Heavier Group 14 (Si-Pb) Dichalcogenolate Carbene Analogues with Sub-9…

2013

The synthesis and spectroscopic and structural characterization of an extensive series of acyclic, monomeric tetrylene dichalcogenolates of formula M(ChAr)2 (M = Si, Ge, Sn, Pb; Ch = O, S, or Se; Ar = bulky m-terphenyl ligand, including two new acyclic silylenes) are described. They were found to possess several unusual features-the most notable of which is their strong tendency to display acute interligand, Ch-M-Ch, bond angles that are often well below 90°. Furthermore, and contrary to normal steric expectations, the interligand angles were found to become narrower as the size of the ligand was increased. Experimental and structural data in conjunction with high-level DFT calculations, in…

Steric effectsMolecular StructureChemistryLigandStereochemistryGeneral ChemistryBiochemistryLondon dispersion forceCatalysischemistry.chemical_compoundCrystallographyColloid and Surface ChemistryMonomerMolecular geometryOrganometallic CompoundsChalcogensQuantum TheoryMoleculeDispersion (chemistry)MethaneCarbeneta116Journal of the American Chemical Society
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Studies on adducts of organotin(IV) halides with bis(acetylacetone)ethylenediimine

1971

The solid state configuration of 1/1 adducts, formed by mono-, di- and tri-organotin(IV) halides with the potentially tetradentate ligand bis(acetylacetone)ethylenediimine, has been investigated. The infrared spectra suggest that the neutral ligand coordinates SnIV through N (or O) atoms of the H-bonded acetylacetoneimine moieties. The skeletal vibrations associated to Sn-C and Sn-Cl bonds are consistent with square planar configurations of the organotin(IV) halide moieties, where SnCl3 and C3Sn groups would be T-shaped, and Alk2SnCl2 would have trans-dialkyl, trans-dichloro arrangements. The latter configuration is supported by the magnitude of the quadrupole splittings. Measurements of th…

LigandAcetylacetoneOrganic ChemistryInorganic chemistrychemistry.chemical_elementInfrared spectroscopyHalideBiochemistryAdductInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Organotin(IV) azido and mixed azidothiocyanato complex anions; A Mössbauer and vibrational spectroscopic study

1975

Abstract Tetraphenylarsonium and tetramethylammonium salts of the complex anions Ph 3 Sn(N 3 ) − 2 , Ph 3 Sn(N 3 )(NCS) − , Me 2 Sn(N 3 ) 2− 4 and Ph 2 Sn(N 3 ) 2 (NCS) 2− 2 have been synthesized, and the solid state configuration of the complex anions has been studied by Mossbauer and vibrational spectroscopies. Trigonal bipyramidal structures are advanced for the Ph 3 Sn IV derivatives, with equatorial SnC 3 and apical pseudohalide ligands, while the R 2 Sn IV compounds are assumed to be trans -octahedral species. The NCS − ligands are observed to be N-bonded to Sn IV . Conductance and PMR (for the Me 2 Sn IV compound) data suggest the presence of the complex anions also in solution phase…

TetramethylammoniumStereochemistryOrganic ChemistrySolid-stateConductanceBiochemistryInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyOctahedronchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Synthesis and structural studies by infrared and Mössbauer spectroscopy of adducts of tin(IV) and organotin(IV) derivatives with 2,2′-azopyridine

1985

Abstract A number of complexes have been prepared by the reaction between 2,2′-azopyridine(AZP) and tin(IV) halides and organotin(IV) halides, and characterized by elemental analysis and infrared and variable temperature 119Sn Mossbauer spectroscopies. All of the new compounds have 1:1 stoichiometry, with the AZP ligand occupying two coordination sites by bonding through one of the ring and one of the azo group nitrogen atoms, to give rise to distorted octahedral structures. In the diorganotin complexes the two organic groups occupy trans positions. The infrared and Mossbauer spectroscopic data suggest that these compounds are monomeric in the solid state.

Azo compoundInfraredLigandInorganic chemistrychemistry.chemical_elementAdductInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinStoichiometryInorganica Chimica Acta
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CCDC 955314: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(bis(mu~2~-eta^6^eta^6^-22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-thiolato)-di-potassium bis(22''66''-tetra-isopropyl-11':3'1''-terphenyl-2'-yl)trisulfane) (bis((22''66''-tetraisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-silicon bromo-bis((22''66''-tetraisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-silicon) dioxane n-hexane solvateExperimental 3D Coordinates
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CCDC 955316: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-tin(ii) tetrahydrofuran solvateExperimental 3D Coordinates
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CCDC 955306: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((22''44''66''-Hexaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-tin toluene solvateExperimental 3D Coordinates
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CCDC 955308: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographybis((22''44''66''-Hexaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-lead(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955309: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal Systembis((22''44'4''66'6''-Octaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-lead benzene solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955315: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Dibromo-bis((22''66''-tetraisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)silane tetrahydrofuran dioxane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955300: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu~2~-eta^6^eta^6^-22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-thiolato)-di-potassium benzene tetrahydrofuran solvateExperimental 3D Coordinates
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CCDC 955298: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographybis((22''44'4''66'6''-Octaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-tin(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955313: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographybis((22''44''66''-Hexaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-siliconCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955302: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((22''44''66''-Hexamethyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-tin(ii)Experimental 3D Coordinates
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CCDC 955312: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersDibromo(bis((22''44''66''-hexaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl))silane hexane solvateExperimental 3D Coordinates
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CCDC 955307: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-yl)triselaneExperimental 3D Coordinates
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CCDC 955303: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal Structurebis((22''44''66''-Hexamethyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-germanium(ii)Cell ParametersExperimental 3D Coordinates
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CCDC 955310: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-yl)selanyl)-tin ((22''66''-tetraisopropyl-11':3'1''-terphenyl-2'-selenenyl chloride) (22''66''-tetraisopropyl-11':3'1''-terphenyl-2'-yl)selane 22''66''-tetraisopropyl-11':3'1''-terphenyl)Experimental 3D Coordinates
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CCDC 955299: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal Systembis(22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-thiolato)-germanium(ii) tetrahydrofuran solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955301: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographybis((22''44'4''66'6''-Octaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-germanium(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 955311: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal Systembis((22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-yl)selanyl)-germanium(ii)Crystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955305: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(22''66''-Tetraisopropyl-11':3'1''-terphenyl-2'-yl)diselaneExperimental 3D Coordinates
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CCDC 955304: Experimental Crystal Structure Determination

2013

Related Article: Brian D. Rekken , Thomas M. Brown , James C. Fettinger , Felicitas Lips , Heikki M. Tuononen , Rolfe H. Herber , and Philip P. Power|2013|J.Am.Chem.Soc.|135|10134|doi:10.1021/ja403802a

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis((22''44''66''-Hexaisopropyl-11':3'1''-terphenyl-2'-yl)sulfanyl)-germanium(ii)Experimental 3D Coordinates
researchProduct