Ph. D. THESIS 2009

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Scheme 9 This equilibrium was investigated using 1 H NMR spectra. The experiments were based on the differences of the chemical shifts for the equatorial protons at positions 2,4,6,8 belonging to the syn (4e,6e = 3.48 ppm) and to the anti isomers (2e,6e = 3.36 ppm). Figure 23. Part 1 H-NMR spectrum of a crude mixture of syn and anti isomers of dioxime 5 The experiments were run starting from either the pure syn or anti isomers and were based on the recording of the 1 H NMR spectra of the same sample over several periods of time and on the measuring in these spectra of the ratios between the isomers using the intensities of their specific signals (Figures 24 and 25). 33
Figure 24. NMR investigation of the antisyn isomerization of 5 Figure 25. NMR investigation of the synanti isomerization of 5. The collecting of data (Table 8) was made at shorter intervals at the beginning of the process and for the calculation of ratios mean values of the integrals were used. 34
Page 1 and 2: “BABES-BOLYAI” UNIVERSITY CLUJ-
Page 3 and 4: General Introduction OUTLINE Part A
Page 5 and 6: 3.6.1. Dots 188 3.6.2. 3D structure
Page 7 and 8: Part A: Synthesis and Structural An
Page 9 and 10: H 3C H 3C O O O C C O O 1a O O C C
Page 11 and 12: The two forms are in equilibrium an
Page 13 and 14: Figu re 4 . Th e 13 C-NMR APT (CDCl
Page 15 and 16: set used , the anarmonicities that
Page 17 and 18: Figure 9. ORTEP diagram for the bic
Page 19 and 20: 1.5.1. Tetramethyl 3,7-dihydroxybic
Page 21 and 22: Table 7. The selected molecular par
Page 23 and 24: a b Figure 14. 1 H NMR spectrum (CD
Page 25 and 26: Figure 16. 13 C NMR spectrum APT (C
Page 27 and 28: Absorbance (a. u.) Absorbance (a.u.
Page 29 and 30: icyclo[3.3.1]nonane-3,7-dione solut
Page 31 and 32: m u lt ip let a t a t δ ==1 .7 6 p
Page 33: Figure 22. 13 C NMR APT spectrum of
Page 37 and 38: (mol·l -1 ) syn 8.8 x10 -3 1.4373
Page 39 and 40: a b Figure 29. 3D FTIR spectra in s
Page 41 and 42: Figure 32. ORTEP diagram for the cy
Page 43 and 44: H2 … N3 = 1.839 Å H5 … N6 = 1.
Page 45 and 46: 2. Conclusions of the part A Differ
Page 47: 20. L. J. Bellamy, “Advanced in I
Page 50 and 51: 2. Experimental part: fabrication a
Page 52 and 53: 3 m 30 m a b Figure 4. Optical imag
Page 54 and 55: (NA 1.25) in phase-contrast (a) and
Page 56 and 57: was chosen instead of an aqueous on
Page 58 and 59: Our goal is to develope a lasser as
Page 60 and 61: Figure 15. a Optical image of gold
Page 62 and 63: the power as parameter exhibits a m
Page 64 and 65: a b Figure 21 a) Optical image of g
Page 66: 4.5.3. 3D structures The 3D structu
Page 69 and 70: Selected References 1. E. S. Wu, J.
Page 71: VIII. J. Bosson-Ehoomann, A. Mihut,

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