Synthetic Attempts towards ‘Aromatic’ Nonafulvenes

According to their spectroscopic behavior, four classes of nonafulvenes may be distinguished, but, so far, only three classes have been identified. Type-A nonafulvenes (including parent 1a) are typically olefinic molecules with strongly alternating bond lengths and a nonplanar nine-membered ring. Type-B nonafulvenes are characterized by four pairs of equivalent ring H-atoms and ring C-atoms. Spectra of both Type-A and Type-B nonafulvenes are not dependent on temperature and solvent polarity. However, spectra of Type-C nonafulvenes (including prototype 1d with R1 = R2 = NMe2) are strongly influenced by temperature and solvent polarity due to an equilibrium 1⇄1± between the nonpolar olefinic 1 and dipolar planarized 1±. So far, Type-D nonafulvenes occurring exclusively in the dipolar form 1± were unknown. Synthetic attempts towards nonafulvenes of Type D are described and problems encountered in nonafulvene syntheses are discussed. Several new cyclononatetraenes and four new nonafulvenes (or nonafulvalenes) 31, 1n, 3, and 5 have been synthesized. Spectroscopic evidence shows that 11,12-bis(diethylamino)nonatriafulvalene 5 is the first Type-D nonafulvene.

[1]  M. Neuenschwander,et al.  11,12‐Bis(diethylamino)nonatriafulvalen, das erste “aromatische” Nonafulven , 1994 .

[2]  M. McAllister,et al.  Fulvenones and isoelectronic diazocyclopolyenes : theoretical studies of structures and stabilization , 1992 .

[3]  M. Neuenschwander,et al.  3J(H,H) Coupling Constants as a Simple Criterion for π Delocalization of Pentafulvenes and Pentafulvalenes† , 1991 .

[4]  M. Neuenschwander,et al.  Nonafulvalen: Synthese durch oxidative Kupplung von Cyclononatetraenid und Valenzisomerisierung , 1987 .

[5]  M. Neuenschwander,et al.  Synthese und NMR-Spektren von Nonafulven sowie Vergleich mit 10-Phenylnonafulven†‡ , 1987 .

[6]  W. Taylor,et al.  Electronic character of methylenecyclopropene: microwave spectrum, structure, and dipole moment , 1986 .

[7]  A. Otter,et al.  1H‐and 13C‐NMR Investigation of Pentafulvenes , 1986 .

[8]  A. Otter,et al.  1H NMR investigation of 10‐dimethylaminononafulvene , 1986 .

[9]  A. Otter,et al.  1H- and 13C-NMR Investigation of Nonafulvenes† , 1986 .

[10]  M. Neuenschwander Synthetic and NMR spectroscopic investigations of fulvenes and fulvalenes , 1986 .

[11]  R. Weiss,et al.  cyclo-C3I4 — die erste salzartige Halogenkohlenstoff-Verbindung† , 1986 .

[12]  M. Neuenschwander,et al.  Synthese neuer Nonafulvene , 1985 .

[13]  G. Sabbioni,et al.  Bis (2,4,6,8‐cyclononatetraen‐1‐yl)methane , 1985 .

[14]  M. Neuenschwander,et al.  Synthese substituierter Cyclononatetraene , 1985 .

[15]  L. J. Schaad,et al.  Ab initio studies on calicene , 1983 .

[16]  W. Thiel,et al.  Aromatizität als Funktion des Ionenpaarcharakters: Akzeptor-substituierte Cyclononatetraenyl-Anionen, Enolat-Anionen mit variablen Ladungsverteilungen und ungewöhnlichen konformativen Eigenschaften , 1982 .

[17]  G. Boche,et al.  Umsetzungen von Akzeptor-substituierten Cyclononatetraenyl-Anionen mit Elektrophilen: Donor-substituierte Nonafulvene und ihre Eigenschaften , 1982 .

[18]  Z. Yoshida Novel pi systems possessing cyclopropenylidene moiety , 1982 .

[19]  G. Boche,et al.  Dynamic equilibrium between ion pairs of aromatic [9]annulene anion and of olefinic nonafulvene structure , 1979 .

[20]  G. Boche,et al.  Darstellung des cis,cis,cis,trans-[9]Annulen-Anions , 1978 .

[21]  G. Boche,et al.  Alkalimetallsalze RC(O)‐substituierter Cyclononatetraenyl‐Anionen: Aromatische [9]Annulen‐Anion‐ oder olefinische Nonafulven‐Struktur als Funktion von Gegenion und Lösungsmittel , 1978 .

[22]  A. Bauder,et al.  The microwave spectrum and dipole moment of heptafulvene , 1976 .

[23]  K. Hafner,et al.  10,10‐Bis(dimethylamino)nonafulvene , 1969 .

[24]  K. Hafner,et al.  Eine einfache Synthese substituierter Fulvene aus 6‐Fulvenyl‐tosylaten , 1968 .

[25]  K. Hafner,et al.  A Simple Synthesis of Substituted Fulvenes from 6‐Fulvenyl p‐Toluenesulfonates , 1968 .

[26]  R. Benson,et al.  Cyclononatetraenide. A Ten-π-Electron Aromatic System , 1965 .

[27]  P. Garratt,et al.  Reactions of the Cyclooctatetraenyl Dianion with gem-Dihalides. The Preparation of Derivatives of Bicyclo [6.1.0]nonatriene. Synthesis of the Cyclononatetraenyl Anion , 1964 .

[28]  K. Hafner,et al.  A Simple Synthesis of Fulvene and Its 6‐Alkyl Derivatives , 1964 .

[29]  K. Hafner,et al.  Eine einfache Synthese des Fulvens und dessen 6‐Alkyl‐Derivaten , 1964 .

[30]  G. Neubauer,et al.  Synthesen mit Amidchloriden, III. Synthese und Reaktionen von Chlorformamidiniumchloriden , 1964 .

[31]  R. Benson,et al.  Cyclononatetraenide. An Aromatic 10-π-Electron System , 1963 .

[32]  P. Garratt,et al.  The Cyclononatetraenyl Anion , 1963 .