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- Page 1 and 2: Synthesis, Characterization, and Ga
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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