Homodiboriranides : the simplest negatively charged homoaromatic compounds

[1]  A. Berndt,et al.  Ein mesitylverbrücktes Methylenboran , 1990 .

[2]  W. Massa,et al.  A Mesityl‐bridged Methyleneborane , 1990 .

[3]  W. Massa,et al.  Structure of a Non‐classically Bridged Methyleneborane in the Crystal , 1990 .

[4]  A. Berndt,et al.  Struktur eines nichtklassisch verbrückten Methylenborans im Kristall , 1990 .

[5]  T. Laube.  X-ray crystal structure analysis of a symmetrically bridged bishomocyclopropenyl cation: 2,3-dimethyl-7-phenyl-2-norbornen-7-ylium hexafluoroantimonate(V) , 1989 .

[6]  W. S. Sheldrick,et al.  Notizen: Darstellung und Kristallstruktur von Cs4Sn2Se6 / Preparation and Crystal Structure of Cs4Sn2Se6 , 1989 .

[7]  W. Massa,et al.  A Monomeric Diboryldilithiomethane with a 1,3‐Diborataallene Structure , 1988 .

[8]  A. Berndt,et al.  Ein monomeres Diboryldilithiomethan mit 1,3-Diborataallen-Struktur , 1988 .

[9]  L. Curtiss,et al.  Intermolecular interactions from a natural bond orbital, donor-acceptor viewpoint , 1988 .

[10]  W. Massa,et al.  Dianion eines Methylendiborirans, Synthese seiner Alkali- und Magnesiumsalze und Struktur seines Dikaliumsalzes / Dianion of a Methylenediborirane, Synthesis of its Alkali and Magnesium Salts and Structure of its Dipotassium Salt , 1988 .

[11]  P. Fagan,et al.  Synthesis of boroles and their use in low-temperature Diels−Alder reactions with unactivated alkenes , 1988 .

[12]  A. Berndt,et al.  Struktur eines Homoborirens / Structure of a Homoborirene , 1988 .

[13]  Warren J. Hehre,et al.  AB INITIO Molecular Orbital Theory , 1986 .

[14]  A. Berndt,et al.  Diboriranide und ein 1,3‐Diboraallyl‐System mit BHB‐Brücke , 1985 .

[15]  H. Schmidbaur.  Chemistry of the Elements. Von N. N. Greenwood und A. Earnshaw. Pergamon Press, Oxford 1984, 1542 S., geb. $ 95.00. ‐ ISBN 0‐08‐022056‐8; Paperback $34.95: ‐ ISBN 0‐08‐022057‐6 , 1985 .

[16]  F. Weinhold,et al.  Natural population analysis , 1985 .

[17]  H. Irngartinger,et al.  Kleine Ringe, 52. Oxidative Ringöffnung von Tetra‐tert‐butyltetrahedran. – Kristall‐ und Molekularstruktur von Tetra‐tert‐butyl‐cyclobutenylium‐Ionen , 1985 .

[18]  R. Bader,et al.  Description of homoaromaticity in terms of electron distributions , 1983 .

[19]  R. Haddon,et al.  MOLECULAR ORBITAL STUDY OF THE HOMOCYCLOPROPENYLIUM CATION , 1983 .

[20]  W. Kutzelnigg.  Theory of Magnetic Susceptibilities and NMR Chemical Shifts in Terms of Localized Quantities , 1982 .

[21]  L. A. Paquette.  Die charakteristischen Eigenschaften homoaromatischer Systeme , 1978 .

[22]  L. Paquette.  The Realities of Extended Homoaromaticity , 1978 .

[23]  G. Olah,et al.  NOVEL AROMATIC SYSTEMS PART 2, CYCLOBUTENYL CATIONS AND THE QUESTION OF THEIR HOMOAROMATICITY, PREPARATION AND STUDY OF THE HOMOCYCLOPROPENIUM ION, THE SIMPLEST HOMOAROMATIC SYSTEM , 1975 .

[24]  Ulrich Fleischer,et al.  The IGLO-Method: Ab-initio Calculation and Interpretation of NMR Chemical Shifts and Magnetic Susceptibilities , 1990 .

[25]  Kenneth B. Wiberg,et al.  Application of the pople-santry-segal CNDO method to the cyclopropylcarbinyl and cyclobutyl cation and to bicyclobutane , 1968 .