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Controlled Morphogenesis of Organic Polyhedral Nanocrystals from Cubes, Cubooctahedrons, to Octahedrons by Manipulating the Growth Kinetics

机译:通过控制生长动力学,从多维数据集,立方八面体到八面体的有机多面体纳米晶体的受控形态发生。

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摘要

Morphological control of organic nanocrystals (ONCs) is important in the fields ranging from specialty chemicals to molecular semiconductors. Although the thermodynamic shape can be readily predicted, most growth morphologies of ONCs are actually determined by kinetic factors and remain poorly understood. On the basis of the reduction of zinc tetraphenylporphyrin perchlorate (ZnTPP+ClO_4~- ) with sodium nitrite (Na~+NO_2~- ), we synthesized two series of ONCs of aquozinc tetraphenylporphyrin (ZnTPP • H_2O), in the presence of either cetyltrimethylammo-nium bromide (CTAB) or poly(vinyl pyrrolidone) (PVP) as the capping ligands. As the cationic precursors of ZnTPP~+ are separated in the solution phase, smoothly controlled release of ZnTPP • H_2O building blocks via the reduction reaction facilitates the separation between the nudeation and growth stages during the formation of ONCs and provides a high and tunable supersaturation unavailable by employing conventional crystallization techniques. We found that CTAB mainly serve as the colloidal stabilizer, while selective adhesion of PVP on the {020} s facet alters the crystal habits significantly. In both cases, manipulation of the growth kinetics had been achieved by adjusting the concentration of ZnTPP • H_2O growth units, and consequently, the supersaturation for the crystallization, thus yielding ONCs with well-controlled sizes and shapes. Remarkably, thermodynamically stable octahedrons have been obtained at high supersaturation in both CTAB and PVP cases.
机译:从特殊化学品到分子半导体,有机纳米晶体(ONC)的形态控制非常重要。尽管可以很容易地预测出热力学形状,但是大多数ONC的生长形态实际上是由动力学因素决定的,并且了解甚少。在亚硝酸钠(Na〜+ NO_2〜-)还原四苯基卟啉高氯酸锌(ZnTPP + ClO_4〜-)的基础上,我们合成了十六烷基三甲基铵中的任何一种四苯基卟啉水合锌(ZnTPP•H_2O)系列。溴化铵(CTAB)或聚乙烯吡咯烷酮(PVP)作为封端配体。由于ZnTPP〜+的阳离子前体在溶液相中分离,通过还原反应平稳控制ZnTPP•H_2O结构单元的释放促进了ONC形成过程中裸相和生长阶段之间的分离,并提供了高而可调的过饱和度通过采用常规的结晶技术。我们发现CTAB主要用作胶体稳定剂,而PVP在{020}面上的选择性粘附会显着改变晶体习性。在这两种情况下,都可以通过调节ZnTPP•H_2O生长单元的浓度,从而调节结晶的过饱和度来控制生长动力学,从而制得大小和形状均受控的ONC。值得注意的是,在CTAB和PVP情况下,都在高过饱和度下获得了热力学稳定的八面体。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第6期|p.1895-1901|共7页
  • 作者单位

    Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People's Republic of China,Graduate University of Chinese Academy of Sciences, Beijing 100039, People's Republic of China;

    Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People's Republic of China;

    Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People's Republic of China,Graduate University of Chinese Academy of Sciences, Beijing 100039, People's Republic of China;

    Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People's Republic of China;

    Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People's Republic of China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:05

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