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相关概念视频

Lattice Centering and Coordination Number02:33

Lattice Centering and Coordination Number

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The structure of a crystalline solid, whether a metal or not, is best described by considering its simplest repeating unit, which is referred to as its unit cell. The unit cell consists of lattice points that represent the locations of atoms or ions. The entire structure then consists of this unit cell repeating in three dimensions. The three different types of unit cells present in the cubic lattice are illustrated in Figure 1.
Types of Unit Cells
Imagine taking a large number of identical...
12.2K
Metallic Solids02:37

Metallic Solids

20.9K
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....
20.9K
Coordination Number and Geometry02:57

Coordination Number and Geometry

19.1K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
19.1K
Coordination Compounds and Nomenclature02:54

Coordination Compounds and Nomenclature

26.9K
In most main group element compounds, the valence electrons of the isolated atoms combine to form chemical bonds that satisfy the octet rule. For instance, the four valence electrons of carbon overlap with electrons from four hydrogen atoms to form CH4. The one valence electron leaves sodium and adds to the seven valence electrons of chlorine to form the ionic formula unit NaCl (Figure 1a). Transition metals do not normally bond in this fashion. They primarily form coordinate covalent bonds, a...
26.9K
Porosity and Absorption of Aggregate01:20

Porosity and Absorption of Aggregate

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Aggregates contain pores of varying sizes; while some are completely enclosed within the particles, others open onto the surface, allowing water to penetrate. The porosity of aggregates is a major factor contributing to the overall porosity of concrete, given that aggregates constitute about three-quarters of concrete's volume.
When all pores in an aggregate are filled with water, the aggregate is considered saturated and surface-dry. If left in dry air, water will evaporate until the...
821
Porosity in Cement Paste01:18

Porosity in Cement Paste

470
The porosity of concrete is a measure of the void spaces within its structure. These spaces impact its strength and durability significantly. When water and cement interact, a chemical reaction called hydration creates a semi-solid paste. This paste includes combined water, making up approximately 23% of the cement's dry mass, and gel water, which fills minuscule voids known as gel pores, accounting for about 28% of the cement gel volume.
The balance of water to cement in the mix is...
470

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相关实验视频

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Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
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协调驱动的自我组装:具有双向多孔性的固体.

Katie Campbell1, Christopher J Kuehl, Michael J Ferguson

  • 1Department of Chemistry, University of Alberta, Edmonton AB T6G 2G2, Canada.

Journal of the American Chemical Society
|June 20, 2002
PubMed
概括
此摘要是机器生成的。

研究人员使用宏观循环的金属导向自组装创建了一个新的多孔材料. 这种材料表现出双向通道,显示出选择性吸收二乙等小型有机客人的潜力.

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Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
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Solid-phase Submonomer Synthesis of Peptoid Polymers and their Self-Assembly into Highly-Ordered Nanosheets
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科学领域:

  • 超分子化学 超分子化学
  • 材料科学 材料科学 材料科学
  • 晶体学 晶体学是指结晶学.

背景情况:

  • 协调驱动的自我组装是创建离散超分子物种和协调聚合物的关键.
  • 形成多孔网络的挑战包括网格相互透,阻碍小分子吸收.
  • 纳米规模的宏观循环提供了一种策略,通过防止相互透来创造多孔固体.

研究的目的:

  • 开发一种双向多孔的固体材料.
  • 为了规避协调聚合物形成中的格子相互透问题.
  • 探索自组装宏循环在创建多孔结构方面的潜力.

主要方法:

  • 使用一种合的宏环联体的金属导向自组装.
  • 描述了溶液和固态中所产生的离散超分子实体.
  • 采用X射线晶体分析来确定固态包装和通道形成.

主要成果:

  • 一个离散的,超分子实体通过金属定向的自我组装成功形成.
  • X射线晶体学证实了组装包可以创建双向通道.
  • 观察到1,2-二乙烯 (ClCH2CH2Cl) 选择性地融入到晶格中.

结论:

  • 合成的材料形成了一个双向多孔的固体.
  • 观察到的双向通道适合选择性吸收小型有机客人.
  • 这种方法提供了一个可行的策略,用于设计有孔的材料,以避免网格相互透.