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[1] H. Schwarz,et al. Elf stabile C5H9+-Kationen in der Gasphase. Zur dissoziativen Ionisierung von 31 isomeren C6H9Br-Verbindungen / Eleven Stable C5H9+ Cations in the Gas Phase. On the Dissociative Ionization of 31 Isomeric C5H9Br Compounds , 1981 .
[2] J. Chandrasekhar,et al. Stable carbocations. 225. Proton and carbon-13 NMR spectroscopic study of 9-fluorenyl cations , 1980 .
[3] J. Chandrasekhar,et al. Dissoziative Ringöffnung halogensubstituierter Methylcyclopropan‐Radikalkationen in der Gasphase , 1980 .
[4] N. Nibbering,et al. Independent existence in the gas phase of the 1-methoxycyclopropyl and 2-methoxyallyl cations, as observed in an ion cyclotron resonance spectrometer , 1979 .
[5] H. Schwarz,et al. Isomerisierung von Methoxy‐ und Carbomethoxysubstituierten Cycloalkyl‐ und Alken‐radikalkationen , 1979 .
[6] H. Schwarz,et al. Ringöffnung CO+- und COOCH3+·-substituierter Cyclopropane und CO-Eliminierung aus isomeren C3H5CO+-Ionen / Ring Opening of CO+ and COOCH3+· Substituted Cyclopropanes and CO Loss from Isomeric C3H5CO+ Ions , 1979 .
[7] M. Ravindranathan,et al. Structural effects in solvolytic reactions. 28. Solvolysis of 1-aryl-1-cyclopropyl 3,5-dinitrobenzoates containing strongly electron-supplying aryl groups. Evidence for two distinct reaction processes involving assisted (K.DELTA.) and unassisted (Kc) mechanisms , 1978 .
[8] G. Bouchoux. Ionisation et fragmentation en spectrométrie de masse VIII. Énergies d'activation de deux fragmentations compétitives, dissociation de l'acétate de phényle et de l'acétanilide sous impact électronique , 1978 .
[9] H. Steinberg,et al. The chemistry of small‐ring compounds. Part 39. Displacements in cyclopropyl chlorides activated by electron‐donating substituents , 1978 .
[10] M. Ravindranathan,et al. Structural effects in solvolytic reactions. 23. New .sigma.+ constants for activating substituents. The solvolysis of 1-aryl-1-cyclopropyl 3,5-dinitrobenzoates containing activating substituents in the aryl group. The tool of increasing electron demand and I-strain , 1977 .
[11] Walter Thiel,et al. Ground States of Molecules. 39. MNDO Results for Molecules Containing Hydrogen, Carbon, Nitrogen, and Oxygen , 1977 .
[12] Walter Thiel,et al. Ground States of Molecules. 38. The MNDO Method. Approximations and Parameters , 1977 .
[13] J. Salauen. 1-Ethynylcyclopropyl tosylate solvolysis. 2. p-Aryl substituent effect upon rate and product distribution , 1977 .
[14] C. Wesdemiotis,et al. Isomerization of hydrocarbon ions. 7. Ring opening reactions in cycloalkane molecular ions. A collisional activation and field ionization kinetic study , 1977 .
[15] D. Seebach,et al. Darstellung und “disproportionierende Hydrolyse” von Cyclopropanonthioacetalen Eine neue Homologisierungsmethode1, 2) , 1976 .
[16] L. Radom,et al. EFFECTS OF SUBSTITUENTS ON THE MECHANISM OF STEREOMUTATION OF ALLYL CATIONS , 1973 .
[17] Ronald A. Martin,et al. Acetolysis of 1-tosyloxy-2,2-dideuteriobicyclopropyl , 1972 .
[18] F. McLafferty,et al. Identification of C3H6.+ structural isomers by ion cyclotron resonance spectroscopy , 1971 .
[19] B. Howell,et al. Synthesis and solvolysis of 1-cyclopropylcyclopropyl tosylate , 1971 .
[20] M. Dewar,et al. Calculated and observed ionization potentials of unsaturated polycyclic hydrocarbons; calculated heats of formation by several semiempirical s. c. f. m.o. methods , 1970, Proceedings of the Royal Society of London. A. Mathematical and Physical Sciences.
[21] J. Eland,et al. Inner Ionization Potentials of Aromatic Compounds , 1968 .
[22] J. Occolowitz,et al. Energetic considerations in the assignment of some fragment ion structures , 1968 .
[23] R. F. Pottie,et al. Free Radicals by Mass Spectrometry. XXIX. Ionization Potentials of Substituted Cyclopentadienyl Radicals , 1963 .
[24] F. Lossing,et al. The Ionization Potentials of the Deuterated Methanes , 1951 .