U. Herzog

发表

Group 14 chalcogenides featuring a bicyclo[3.3.0]octane skeleton

U. Böhme, E. Brendler, G. Rheinwald, 2001 .

Interactions of chloromethyldisilanes with tetrakis(dimethylamino)ethylene (TDAE), formation of [TDAE]+ [Si3Me2Cl7]−

H. Lang, E. Brendler, G. Roewer, 2002 .

BASE CATALYSED HYDROGENATION OF METHYLBROMOOLIGOSILANES WITH TRIALKYLSTANNANES, IDENTIFICATION OF THE FIRST METHYLBROMOHYDROGENOLIGOSILANES

G. Roewer, U. Herzog, 1997 .

Bis(oligosilanyl)chalcogenides [(Me3Si)xMe3−xSi]2E, alkalimetal oligosilanylchalcogenolates (Me3Si)xMe3−xSiEMI and oligosilanylchalcogenols (Me3Si)xMe3−xSiEH (E=S, Se, Te)

U. Herzog, H. Lange, 2002 .

3,7,10‐Trichalcogenaoctasila[3.3.3]propellanes

G. Rheinwald, U. Herzog, 2001 .

Silicon Carbide — A Survey of Synthetic Approaches, Properties and Applications

K. Trommer, E. Müller, S. Frühauf, 2002 .

Organosilicon Halides—Synthesis and Properties

U. Herzog, 2009 .

Organosilicon chalcogenides with trisilane units – bicyclo[3.3.1]nonanes, bicyclo[3.2.2]nonanes and spiro[4.4]nonanes

H. Borrmann, U. Herzog, 2004 .

Preparation of oligosilanes containing perhalogenated silyl groups and their hydrogenation by stannanes

G. Roewer, U. Herzog, 1997 .

Methylchlorooligosilanes as products of the basecatalysed disproportionation of various methylchlorodisilanes

E. Brendler, G. Roewer, U. Herzog, 1996 .

Bicyclo[2.2.2]octanes HC(SiMe2E)3MR (E=S, Se; M=Si, Ge, Sn; R=Me, Ph, Vi)

H. Borrmann, G. Rheinwald, U. Herzog, 2002 .

Organosilicon hypersilylchalcogenolates and related compounds

H. Borrmann, B. Walfort, U. Herzog, 2004 .

Novel Chalcogenides of Silicon with Bicyclo[2.2.2]octane Skeletons, MeSi(SiMe2E)3MR (E = S, Se, Te; M = Si, Ge, Sn; R = Me, Ph)

G. Rheinwald, U. Herzog, 2001 .

New chalcogen derivatives of silicon possessing adamantane and noradamantane structures

G. Rheinwald, U. Herzog, 2001 .

Synthesis and characterization of 2,5,7-trichalcogena-1,3,4,6-tetrasilanorbornanes (RMeSiSiMe)2E3 (R=Me, Ph/E=S, Se, Te)

U. Böhme, G. Rheinwald, U. Herzog, 2001 .

Five- and six-membered ring Group 14 chalcogenides of the types (Me2ME)3 (M=Si, Ge, Sn), E(Si2Me4)2E, Me4Si2(E)2MRx (MRx=C(CH2)5, SiMe2, GeMe2, SnMe2, SnPh2, BPh) and [Me4Si2(E)2SiMe]2 (E=S, Se, Te)

G. Rheinwald, U. Herzog, 2001 .

SYNTHESIS AND NMR INVESTIGATIONS OF TELLUROBUTYL-SUBSTITUTED SILANES

U. Herzog, 2001 .

Formation and characterization of cyclic and polycyclic silthianes containing Si Si bonds

H. Lang, U. Böhme, G. Roewer, 2000 .

Preparation and 29Si NMR spectroscopical investigations of (diethylamino)‐methylchlorotetra‐ and pentasilanes

K. Trommer, G. Roewer, U. Herzog, 1997 .

SYNTHESIS AND NMR INVESTIGATIONS ON BUTYLTHIOSUBSTITUTED MONO- AND OLIGOSILANES

G. Roewer, U. Herzog, 1999 .

Molecular structures of trimeric diphenyltin chalcogenides, (Ph2SnE)3, E = S, Se, Te

U. Böhme, G. Rheinwald, U. Herzog, 2002 .

Silicon-lead chalcogenides of the types Me4Si2(E)2PbPh2 and Ph2Pb(E)2Si2Me2(E)2PbPh2 (E=S, Se) and related compounds containing tin and antimony

G. Rheinwald, U. Herzog, 2002 .

Synthesis and NMR Investigation of Selenobutyl Substituted Silanes and Oligosilanes

U. Herzog, 2000 .

Organosilicon chalcogenides with trisilane units - adamantanes and noradamantanes

H. Borrmann, U. Herzog, 2003 .

Heteronoradamantanes Me2Si2(RM)2E5 (RM = MeGe, PhSn; E = S, Se)

H. Borrmann, U. Herzog, 2003 .

New Cyclic and Polycyclic Ring Systems Containing Group 14 (Si, Ge, Sn) and 16 (S, Se, Te) Elements

U. Böhme, G. Rheinwald, U. Herzog, 2001 .

Dimeric and trimeric diorganosilicon chalcogenides (PhRSiE)2,3 (E = S, Se, Te; R = Ph, Me)

H. Borrmann, H. Lang, B. Walfort, 2004 .

MODIFICATION OF THE BASE-CATALYSED DISPROPORTIONATE OF METHYLCHLORODIflLANES

G. Roewer, U. Herzog, Ν. Schulze, 1999 .

Tetrakis(trimethylsilyl)cyclodisilthiane and -selenane

H. Borrmann, U. Herzog, 2003 .

SYNTHESIS OF CYCLOALKYL SUBSTITUTED CYCLOTETRASILANES

G. Roewer, G. Rheinwald, U. Herzog, 2002 .

1.4-Addition of 1.1.2.2-tetrachlorodimethyldisilane to 1.4-diaza-1.3-dienes, synthesis and molecular structure of 1.6-disila-2.5-diaza-1.1.6.6-tetrachloro-1.6-dimethyl-2.5-di-p-tolyl-3.4-diphenyl-hexa-3-ene

B. Ziemer, G. Roewer, U. Herzog, 1997 .