- Page 1: Synthesis, Characterization, and Ga
- Page 5 and 6: General Introduction cellulose deri
- Page 7 and 8: General Introduction biogenetically
- Page 9 and 10: General Introduction chemistry offe
- Page 11 and 12: General Introduction solution-diffu
- Page 13 and 14: General Introduction A simplified t
- Page 15 and 16: General Introduction been observed
- Page 17 and 18: polymers. 41,46 General Introductio
- Page 19 and 20: General Introduction Keeping in vie
- Page 21 and 22: General Introduction the derivatize
- Page 23 and 24: General Introduction strategy (G1-a
- Page 25 and 26: General Introduction In conclusion,
- Page 27 and 28: General Introduction 5. (a) Kobayas
- Page 29 and 30: General Introduction 15. (a) Goetma
- Page 31 and 32: General Introduction American Chemi
- Page 33 and 34: General Introduction Macromolecules
- Page 35 and 36: Silylation of Ethyl Cellulose Intro
- Page 37 and 38: Silylation of Ethyl Cellulose milli
- Page 39 and 40: Silylation of Ethyl Cellulose chlor
- Page 41 and 42: Silylation of Ethyl Cellulose Resul
- Page 43 and 44: Silylation of Ethyl Cellulose Solub
- Page 45 and 46: Silylation of Ethyl Cellulose 1.034
- Page 47 and 48: Silylation of Ethyl Cellulose poly(
- Page 49 and 50: Silylation of Ethyl Cellulose the r
- Page 51 and 52: Silylation of Ethyl Cellulose D.; Y
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Chapter 2 51 Chapter 2 Synthesis, C
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53 Chapter 2 are few and far betwee
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55 Chapter 2 constant volume/variab
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57 Chapter 2 Membrane Density. Memb
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59 Chapter 2 IR spectrum of 1 (Figu
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61 Chapter 2 1,3-bis(trifluoromethy
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63 Chapter 2 The increase in the po
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65 Chapter 2 other fluorinated poly
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67 Chapter 2 of the gas permeabilit
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69 Chapter 2 Gas Diffusivity and So
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71 Chapter 2 mobility of the perflu
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73 Chapter 2 1325-1329. (b) Hamza,
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Chapter 3 75 Chapter 3 Synthesis an
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77 Chapter 3 cost, and above all ap
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79 Chapter 3 molecular weights (Mn
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81 Chapter 3 1.99-2.07 (m, 2H, (CH3
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83 Chapter 3 25 °C, ppm): 11.9, 13
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85 Chapter 3 38.1, 44.7, 46.8, 47.9
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87 Chapter 3 CH2CH2C(=O)O), 2.50-4.
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89 Chapter 3 1091, 1053, 853, 806,
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91 Chapter 3 dendrons (G1-a-ІІ-G1
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93 Chapter 3 (DMAP) as a base, as s
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Figure 3. FTIR spectra of 1, 2c, an
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97 Chapter 3 (partly soluble) and 3
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99 Chapter 3 increased polarity of
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101 Chapter 3 that of 1, and approx
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103 Chapter 3 derivatization per th
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105 Chapter 3 (2a-c) were in the or
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107 Chapter 3 2709-2719. (b) Schenn
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109 Chapter 3 17. van Krevelen, D.
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Chapter 4 111 Chapter 4 Synthesis,
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113 Chapter 4 Since, no significant
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115 Chapter 4 Materials. Ethyl cell
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DStotal = DSEt + DSCarb (for 1a and
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119 Chapter 4 Figure 2. 1 H NMR spe
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121 Chapter 4 ruling out the possib
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123 Chapter 4 t-butyl moiety. A str
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125 Chapter 4 reported to lead to t
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127 Chapter 4 Table 4. Gas Permeabi
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129 Chapter 4 augmentation in eithe
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131 Chapter 4 indicate the signific
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133 Chapter 4 M.-R. J. Appl. Polym.
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Chapter 5 135 Chapter5 Synthesis an
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137 Chapter5 acid- and peptide-cont
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139 Chapter5 Specific rotations ([
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141 Chapter5 1.66 (brs, 1.1H, NHCH(
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143 Chapter5 as shown in Scheme 1,
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145 Chapter5 in Table 1. The molecu
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147 Chapter5 almost same pattern of
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Conclusions Table 3. Thermal Proper
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151 Chapter5 W.; Jing, X. J. Polym.
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Chapter 5 Synthesis and Properties
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Acknowledgments While submitting th
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Synthesis, Characterization, and Ga