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Pure Appl. Chem., 1984, Vol. 56, No. 1, pp. 151-162

http://dx.doi.org/10.1351/pac198456010151

Remarkable structures of lithium compounds

P. Rague von Schleyer

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  • Schade Christian, von Ragué Schleyer Paul, Gregory Peter, Dietrich Hans, Mahdi Waruno: Competition among multihapto bonding, solvation, and aggregation. The η1/η2 infinite-chain X-ray structure of indenylsodium · N,N,N′,N′-tetramethyl-1,2-diaminoethane. J Organomet Chem 1988, 341, 19. <http://dx.doi.org/10.1016/0022-328X(88)89060-0>
  • Setzer Willlam N., von Ragué Schleyer Paul, Mahdi Waruno, Dietrich Hans: The crystal structure of the reaction product of n-butyllithium with 7,8-benzoquinoline. Tetrahedron 1988, 44, 3339. <http://dx.doi.org/10.1016/S0040-4020(01)85967-6>
  • Müllen Klaus: Neue reduktive Umwandlungen cyclischer ungesättigter Kohlenwasserstoffe. Angew Chem 1987, 99, 192. <http://dx.doi.org/10.1002/ange.19870990306>
  • Bickelhaupt Friedrich: Di-Grignard-Verbindungen und Metallacyclen. Angew Chem 1987, 99, 1020. <http://dx.doi.org/10.1002/ange.19870991007>
  • Günther Harald, Moskau Detlef, Bast Peter, Schmalz Dietmar: Moderne NMR-Spektroskopie von Organolithium-Verbindungen. Angew Chem 1987, 99, 1242. <http://dx.doi.org/10.1002/ange.19870991205>
  • Hacker Roland, Kaufmann Elmar, von Ragué Schleyer Paul, Mahdi Waruno, Dietrich Hans: Die Röntgenstruktur vonN-Lithiocarbazol-Dimer: Experimentelle Bestätigung der theoretischen Analyse von Strukturen desN-Lithiopyrrol-Typs. Chem Ber 1987, 120, 1533. <http://dx.doi.org/10.1002/cber.19871200911>
  • Wrackmeyer Bernd, Abu-Orabi Sultan T.: (E)/(Z)-Isomerisierung von 1-Boryl-2-stannyl-1-alkenen. Chem Ber 1987, 120, 1603. <http://dx.doi.org/10.1002/cber.19871200922>
  • Jaworski Andrzej, Person Willis B., Adamowicz Ludwik, Bartlett Rodney J.: Study of the conformation of the dilithioacetylene molecule. Int J Quantum Chem 1987, 32, 613. <http://dx.doi.org/10.1002/qua.560320762>
  • Busch Marianna A., Harlow Richard, Watson Patricia L.: Unusual eight-membered rings with linear symmetric methyl groups from yttrium and lutetium methyl complexes. Inorg Chim Ada 1987, 140, 15. <http://dx.doi.org/10.1016/S0020-1693(00)81038-5>
  • Schleyer Paul Von Ragué, Kaufmann Elmar, Kos Alexander J., Clark Timothy, Pople John A.: 1,2-Dilithioethen-Isomere und die Mechanismen ihrer gegenseitigen Umwandlung, eine ab-initio-Untersuchung. Angew Chem 1986, 98, 164. <http://dx.doi.org/10.1002/ange.19860980207>
  • Hoppe Dieter, Krämer T.: α-Deprotonierung eines α-chiralen 2-Alkenylcarbamats unter Retention und Lithium-Titan-Austausch unter Inversion - zur Homoaldol-Reaktion unter 1,3-Chiralitätsübertragung. Angew Chem 1986, 98, 171. <http://dx.doi.org/10.1002/ange.19860980212>
  • von Schnering Hans Georg, Schwarz Martin, Nesper Reinhard: Rote, transparente Alkalimetallsilicide mit Si4-Tetraedern. Angew Chem 1986, 98, 558. <http://dx.doi.org/10.1002/ange.19860980616>
  • Schade Christian, Schleyer Paul Von Ragué, Geißler Maren, Weiss Erwin: Die Struktur eines Propadienylnatrium-Derivats – Konkurrenz zwischen Ladungsdelokalisierung durch Resonanz und Ladungslokalisierung durch das Gegenion. Angew Chem 1986, 98, 922. <http://dx.doi.org/10.1002/ange.19860981022>
  • Hoppe Dieter, Krämer Thomas: α-Deprotonation of an α-Chiral 2-Alkenylcarbamate with Retention and Lithium-Titanium Exchange with Inversion— the Homoaldol Reaction with 1,3-Chirality Transfer. Angew Chem Int Ed Engl 1986, 25, 160. <http://dx.doi.org/10.1002/anie.198601601>
  • Schleyer Paul von Ragué, Kaufmann Elmar, Kos Alexander J., Clark Timothy, Pople John A.: 1,2-Dilithioethylene Isomers and Their Mechanisms of Interconversion: an Ab Initio Study. Angew Chem Int Ed Engl 1986, 25, 169. <http://dx.doi.org/10.1002/anie.198601691>
  • Schade Christian, Schleyer Paul von Ragué, Weiss Erwin, Geissler Maren: The Structure of an Allenylsodium Derivative—Competition between Carbanion Resonance Delocalization and Gegenion Charge Localization. Angew Chem Int Ed Engl 1986, 25, 902. <http://dx.doi.org/10.1002/anie.198609021>
  • Farrǵs Jaume, Olivella Santiago, Solé Albert, Vilarrasa Jaume: Substituent Effects on the Low-Lying Singlet and Triplet States of Methylene. J Comput Chem 1986, 7, 428. <http://dx.doi.org/10.1002/jcc.540070406>
  • Von Ragué Schleyer Paul, Sawaryn Andrzej, Reed Alan E., Hobza Pavel: The Remarkable Structure of Lithium Cyanide/Isocyanide. J Comput Chem 1986, 7, 666. <http://dx.doi.org/10.1002/jcc.540070509>
  • Schiffer Heinz, Ahlrichs Reinhart: The C-Li bond in methyllithium. Binding energy and ionic character. chem phys letts 1986, 124, 172. <http://dx.doi.org/10.1016/0009-2614(86)85138-7>
  • J. Brauer David, Hietkamp Sibbele, Stelzer Othmar: Crystal structure of bis(diphenylphosphino)-methyllithium (N,N,N′,N′-tetramethylethylenediamine): An organolithium compound without lithium—carbon bonding. J Organomet Chem 1986, 299, 137. <http://dx.doi.org/10.1016/0022-328X(86)82008-3>
  • Hacker Roland, von Rague Schleyer Paul, Reber Gabriele, Müller Gerhard, Brandsma Lambert: 2,6-Bis(lithiumtrimethylsilylmethyl)pyridine · 2TMEDA: A monomeric dilithio compound exhibiting electrostatic charge communication. J Organomet Chem 1986, 316, C4. <http://dx.doi.org/10.1016/0022-328X(86)82094-0>
  • Rücker Christoph: Multiply metallated organic intermediates: a tris(lithiomethyl)cyclohexane and a hexalithiotrimethylcyclohexanetriolate. J Organomet Chem 1986, 310, 135. <http://dx.doi.org/10.1016/S0022-328X(00)99547-0>
  • von Rague Schleyer Paul, Spitznagel Günther H., Chandrasekhar Jayaraman: The ethyl, 1- and 2-propyl, and other simple alkyl “carbanions” do not exist. Tetrahetron Lett 1986, 27, 4411. <http://dx.doi.org/10.1016/S0040-4039(00)84965-5>
  • Vollhardt Jürgen, Gais Hans-Joachim, Lukas Karl L.: Dilithio(phenylsulfonyl)trimethylsilylmethan: Synthese,13C/1H-NMR-Charakterisierung und Lithium-Titan-Austausch. Angew Chem 1985, 97, 695. <http://dx.doi.org/10.1002/ange.19850970815>
  • Boche Gernot, Etzrodt Heinz, Massa Werner, Baum Gerhard: Polymorphie bei einer Organolithium-Verbindung: Dilithium-1,2-diphenyl-benzocyclobutadien-diid· 2 Tetramethylendiamin. Angew Chem 1985, 97, 858. <http://dx.doi.org/10.1002/ange.19850971012>
  • Vollhardt Jürgen, Gais Hans-Joachim, Lukas Karl L.: Dilithio(phenylsulfonyl)trimethylsilylmethane: Synthesis, 13C/1H-NMR Characterization, and Lithium-Titanium Exchange. Angew Chem Int Ed Engl 1985, 24, 696. <http://dx.doi.org/10.1002/anie.198506961>
  • Boche Gernot, Etzrodt Heinz, Massa Werner, Baum Gerhard: Polymorphism of an Organolithium Compound: Dilithium 1,2-diphenylbenzocyclobutadienediide · 2 Tetramethylethylenediamine. Angew Chem Int Ed Engl 1985, 24, 863. <http://dx.doi.org/10.1002/anie.198508631>
  • Neugebauer Wolfgang, Geiger Gottfried A. P., Kos Alexander J., Stezowski John J., von Ragué Schleyer Paul: Erzeugung von Cumulenen durch Lithium-Addition an 1,3-Diine. Röntgenstruktur von [3,6-Di(lithio-THF)-2,2,7,7-tetramethyl-3,4,5-octatrien]2, einem 1,4-Dilithiobutatrien-Dimeren. Chem Ber 1985, 118, 1504. <http://dx.doi.org/10.1002/cber.19851180418>
  • Becker G., Hartmann H.-M., Münch A., Riffel H.: Synthese und Struktur von Lithium-tris(trimethylsilyl)silanid · 1,5 DME. Z anorg allg Chem 1985, 530, 29. <http://dx.doi.org/10.1002/zaac.19855301104>
  • Kos Alexander J., Stein Peter, von Ragué Schleyer Paul: The doubly bridged structure of 1,4-dilithio-cis-2-butene. A theoretical demonstration of the importance of counter-ion effects and of lithium multicenter bonding. J Organomet Chem 1985, 280, C1. <http://dx.doi.org/10.1016/0022-328X(85)87073-X>
  • Wilhelm Dieter, Clark Timothy, von Ragué Schleyer Paul, Dietrich Hans, Mahdi W.: Double lithium bridging: The structure of 1,4-dilithio-1,4-diphenyl-cis-2-butene. J Organomet Chem 1985, 280, C6. <http://dx.doi.org/10.1016/0022-328X(85)87074-1>
  • Armstrong D.R., Perkins P.G., Walker G.T.: The electronic structure of the monomers, dimers, a trimer, the oxides and the borane complexes of the lithiated ammonias. Journal of Molecular Structure: THEOCHEM 1985, 122, 189. <http://dx.doi.org/10.1016/0166-1280(85)80080-4>
  • Mills R.J., Horvath R.F., Sibi M.P., Snieckus V.: Dilithiated synthons of tertiary benzamides, phthalamides, and 0,0′-aryl dicarbamates. Tetrahetron Lett 1985, 26, 1145. <http://dx.doi.org/10.1016/S0040-4039(00)98418-1>