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新型树枝状大分子,其包含一个共价连接到Newkome树枝状分子顶端位置的单钴茂单元:电化学及与葫芦[7]脲的客体结合相互作用

New dendrimers containing a single cobaltocenium unit covalently attached to the apical position of Newkome dendrons: electrochemistry and guest binding interactions with cucurbit[7]uril.

作者信息

Sobransingh David, Kaifer Angel E

机构信息

Center for Supramolecular Science and Department of Chemistry, University of Miami, Coral Gables, Florida 33124-0431, USA.

出版信息

Langmuir. 2006 Dec 5;22(25):10540-4. doi: 10.1021/la061188o.

Abstract

Two new dendrimer series were prepared and characterized. These dendrimers contain a single bis(cyclopentadienyl)cobalt(III) (cobaltocenium, Cob+) unit covalently attached to the apical (focal) position of Newkome-type dendrons, ranging in size from first to third generation. The dendrimers in the first series (1ECob+-3ECob+) are hydrophobic and have 3, 9, and 27 tert-butyl esters on their peripheries, whereas the dendrimers in the second series (1Cob+-3Cob+) are hydrophilic with 3, 9, and 27 carboxylic acid groups on their surfaces, respectively. In voltammetric experiments, all dendrimers showed the expected one-electron reversible reduction of the cobaltocenium center, and the heterogeneous rate of electron transfer decreased with generation in both dendrimer series. The host-guest binding interactions between water-soluble dendrimers 1Cob+-3Cob+ and the cucurbit[7]uril (CB7) host were investigated using 1H NMR spectroscopy, MALDI-TOF mass spectrometry, and electrochemical techniques. The association equilibrium constants (K) for all dendrimer guests were significantly lower than that measured for the inclusion complex between underivatized Cob+ and CB7 (K = 5.7 x 10(9) M(-1)). Nonetheless, among the three dendrimers surveyed, the second-generation dendrimer, 2Cob+, afforded optimum stabilization for the CB7 inclusion complex.

摘要

制备并表征了两个新型树枝状聚合物系列。这些树枝状聚合物包含一个单双(环戊二烯基)钴(III)(钴茂,Cob +)单元,该单元共价连接到Newkome型树枝状分子的顶端(焦点)位置,尺寸范围从第一代到第三代。第一个系列(1ECob + -3ECob +)中的树枝状聚合物是疏水的,其外围分别有3个、9个和27个叔丁酯,而第二个系列(1Cob + -3Cob +)中的树枝状聚合物是亲水的,其表面分别有3个、9个和27个羧酸基团。在伏安实验中,所有树枝状聚合物都显示出钴茂中心预期的单电子可逆还原,并且两个树枝状聚合物系列中的电子转移异相速率均随代数降低。使用1H NMR光谱、基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)和电化学技术研究了水溶性树枝状聚合物1Cob + -3Cob +与葫芦[7]脲(CB7)主体之间的主客体结合相互作用。所有树枝状聚合物客体的缔合平衡常数(K)均明显低于未衍生化的Cob +与CB7之间的包合物所测得的平衡常数(K = 5.7 x 10(9) M(-1))。尽管如此,在所研究的三种树枝状聚合物中,第二代树枝状聚合物2Cob +为CB7包合物提供了最佳稳定性。

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