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第4组八面体胺酸复合物:在压力调节的烯聚合过程中的合成,结构和催化作用
Victoria Volkis1, Elza Nelkenbaum, Anatoli Lisovskii
1Department of Chemistry, Institute of Catalysis Science and Technology, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Journal of the American Chemical Society
|February 20, 2003
概括
第4组金属的胺酸复合物催化了烯聚合,压力控制了聚合物的战术性,从攻击性到异攻击性. 催化剂结构和共催化剂显著影响活性和立体规律性.
科学领域:
- 有机金属化学 有机金属化学
- 聚合物化学 聚合物化学
- 催化剂是一种催化剂.
背景情况:
- 胺酸联体为金属复合体合成提供可调节的硬质和电子特性.
- 第4组金属复合物被广泛探索为烯聚合物的催化剂.
研究的目的:
- 合成和表征胺酸联体和4组金属复合物.
- 研究这些复合物在烯聚合过程中的催化活性.
- 了解反应条件和复杂结构如何影响聚合物微观结构.
主要方法:
- 合成和X射线衍射研究的本扎米丁酸复合物.
- 使用MAO或B的烯聚合实验.
- 分析聚合物微结构 (战术性,立体规律性) 作为反应参数的函数.
主要成果:
- 合成了Zr和Ti的八面体胺酸复合物.
- 催化剂活性和立体规律性是由压力,溶剂和共催化剂调节的.
- 复合体9与B(C(6) F(5)))) 3) 产生了高度异性聚烯 (98% mmmm).
- 综合体10在高压下生产了弹性聚烯.
- 弹性体表现出交替的异态域和由于表皮化而导致的立体缺陷.
结论:
- 胺酸复合物是用于立体正规烯聚合的多功能催化剂.
- 压力是控制聚合物战术性的关键参数.
- 复杂的结构和共催化剂的选择对于实现所需的聚合物特性至关重要.
相关概念视频
Carboxylic Acid Derivatives: Overview
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Structures of Carboxylic Acid Derivatives
Structure of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Preparation of Acid Anhydrides
One of the methods for preparing symmetrical or unsymmetrical acid anhydrides involves the treatment of acid chlorides with the sodium salt of carboxylic acids. The reaction proceeds via a nucleophilic acyl substitution.
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
Five-Membered Heterocyclic Aromatic Compounds: Overview
Heterocyclic aromatic compounds are cyclic compounds that are aromatic and have one or more heteroatoms—atoms other than carbon, in the ring. Depending upon the number of atoms present in the ring, they can be either five or six-membered. Examples of five-membered heterocyclic aromatic compounds include pyrrole, furan, thiophene, and imidazole. Pyrrole consists of one nitrogen atom having one lone pair of electrons. Furan and thiophene have one oxygen and one sulfur heteroatom, respectively.
Polymer Classification: Architecture
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
Polymer Classification: Stereospecificity
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...

