首页> 外文学位 >Part I: Self-assembling dendrimers using the DDA-AAD hydrogen bonding motif. Part II: Supramolecular discotic liquid crystals through hydrogen bond mediated self-assembly.
【24h】

Part I: Self-assembling dendrimers using the DDA-AAD hydrogen bonding motif. Part II: Supramolecular discotic liquid crystals through hydrogen bond mediated self-assembly.

机译:第一部分:使用DDA-AAD氢键基序的自组装树状聚合物。第二部分:超分子盘状液晶通过氢键介导的自组装。

获取原文
获取原文并翻译 | 示例

摘要

In part I, a heterocyclic unit which contains complementary donor-donor-acceptor (DDA) and acceptor-acceptor-donor (AAD) (G·C-like) hydrogen bonding arrays at an angle of about 60° was used to self-assemble dendrimers into a hexamer. To investigate its ability to self-assemble higher generation dendrimers, second and third generation Fréchet-type dendron were attached to the 8-amino group the 2,8-diamino-2-N-ethylpyrimido-(4,5- b)[1,8] naphthyridine-3H-4-one subunit. Studies using 1H NMR, size exclusion chromatography (SEC) and dynamic light scattering (DLS) support the cooperative formation of cyclic hexamers in apolar solvents. The stability of the self-assembled dendrimers is dependent on the size of the attached dendron. Pair-wise mixing studies with different generation dendritic monomers indicate their usefulness in constructing dynamic combinatorial libraries.; In part II, the ability of this heterocyclic unit to generate a self-assembled structure in bulk was tested by attachment of a 3,4,5-tris-dodecyloxybenzyl group to the 8-amino group and evaluating the mesomorphic properties of the resulting derivative. Cumulative solution studies by 1H NMR, SEC and DLS indicate the formation of a hydrogen bonded cyclic hexamer in apolar solvents. The studies by differential scanning calorimetry (DSC), polarized light microscopy (PLM) and X-ray diffraction (XRD) indicate that the hexameric disks can stack in bulk to form thermotropic columnar mesophases. The mesophases exist across a large temperature range (>248°C).
机译:在第一部分中,使用含有互补供体-供体-受体(DDA)和受体-受体-供体(AAD)(类G·C)氢键阵列的杂环单元自组装树枝状聚合物变成六聚体。为了研究其自组装高级树状聚合物的能力,将第二和第三代Fréchet型树突连接到2,8-二氨基-2- N -乙基嘧啶-(4 ,5- b )[1,8]萘啶-3 H -4-one亚基。使用 1 NMR,尺寸排阻色谱法(SEC)和动态光散射(DLS)进行的研究支持在非极性溶剂中协同形成环状六聚体。自组装树枝状聚合物的稳定性取决于所附着树枝状分子的大小。与不同代树突状单体的成对混合研究表明它们在构建动态组合文库中的有用性。在第二部分中,通过将3,4,5-三十二烷基氧基苄基连接到8-氨基并评估所得衍生物的介晶性质,测试了该杂环单元整体上产生自组装结构的能力。 。通过 1 NMR,SEC和DLS进行的累积溶液研究表明,在非极性溶剂中形成了氢键合的环状六聚体。通过差示扫描量热法(DSC),偏振光显微镜(PLM)和X射线衍射(XRD)进行的研究表明,六聚体盘可以大量堆积以形成热致柱状中间相。中间相存在于较大的温度范围(> 248°C)。

著录项

  • 作者

    Ma, Yuguo.;

  • 作者单位

    University of Illinois at Urbana-Champaign.;

  • 授予单位 University of Illinois at Urbana-Champaign.;
  • 学科 Chemistry Organic.; Chemistry Polymer.; Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 128 p.
  • 总页数 128
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;高分子化学(高聚物);工程材料学;
  • 关键词

  • 入库时间 2022-08-17 11:45:53

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号