碳水化合物棒结合物:三元棒-卷子分子形成复杂的液晶结构
Bin Chen1, Ute Baumeister, Gerhard Pelzl
1Institute of Organic Chemistry, University Halle, Kurt-Mothes-Strasse 2, D-06120 Halle, Germany.
Journal of the American Chemical Society
|November 25, 2005
概括
新型T形分子自组织成独特的液晶相,包括具有三维周期子空间的网络结构. 这些发现促进了对复杂材料自组装和相位行为的理解.
科学领域:
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
- 液晶是一种液晶.
背景情况:
- 形T的多性triblock分子结合了棒状,水性和脂性细分.
- 了解它们的自我组织是设计先进材料的关键.
研究的目的:
- 合成新型T形多性三阻分子.
- 研究它们的热热流体液晶行为和自我组织模式.
- 探索分子结构对相位形成的影响.
主要方法:
- 催化交叉合反应用于合成.
- 极化光显微镜,差分扫描热量计 (DSC) 和X射线散射用于表征.
- 极性和脂性细分长度的系统变化.
主要成果:
- 发现了不寻常的液晶相,包括六角通道层 (ChL(hex)) 和蜂状网络 (方形/五角形圆柱体).
- 一个六角柱状相的观测与触角烯基核心组织.
- 在一个化合物中由于基核心重定向而导致的双折反转.
- 在添加前性溶剂时诱导状相.
结论:
- 分子架构要求复杂的自我组织成为独特的3D周期性液晶相.
- 这些材料表现出不同的相位行为,取决于细分长度和溶剂相互作用.
- 这些发现为设计具有量身定制超分子结构的材料提供了洞察力.
相关概念视频
Molecular Models
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
Structures of Solids
Solids in which the atoms, ions, or molecules are arranged in a definite repeating pattern are known as crystalline solids. Metals and ionic compounds typically form ordered, crystalline solids. A crystalline solid has a precise melting temperature because each atom or molecule of the same type is held in place with the same forces or energy. Amorphous solids or non-crystalline solids (or, sometimes, glasses) which lack an ordered internal structure and are randomly arranged. Substances that...
Ionic Crystal Structures
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Metallic Solids
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
Network Covalent Solids
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
Vicinal or three-bond coupling is commonly observed between protons attached to adjacent carbons. Here, nuclear spin information is primarily transferred via electron spin interactions between adjacent C‑H bond orbitals. This generally favors the antiparallel arrangement of spins, so 3J values are usually positive.
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...


