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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Two-dimensional self-assembly and phase behavior of an alkoxylated sandwich-type bisphthalocyanine and its phthalocyanine analogues at the liquid-solid interface
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Two-dimensional self-assembly and phase behavior of an alkoxylated sandwich-type bisphthalocyanine and its phthalocyanine analogues at the liquid-solid interface

机译:烷氧基化夹心型双酞菁及其酞菁类似物在液-固界面处的二维自组装和相行为

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Lanthanide bisphthalocyanine complexes are interesting objects for the construction of two-dimensional (2D) ordered arrays with prospective applications in molecular electronics due to their unique semiconductor and electrochromic properties as well as their double-decker architecture. The 2D self-assembly of dodecyloxy-substituted (bisphthalocyaninato)erbium(III) has been studied at the solid (highly oriented pyrolytic graphite)-liquid interface by scanning tunneling microscopy. The results show that the bisphthalocyanine molecules form an ordered quadratic 2D lattice (alpha = b = 3.0 +/- 0.+/- 1 nm, gamma = 3 degrees), which is nearly identical to that formed by its (phthalocyaninato)cobalt(H) analogue bearing alkoxy chains of the same length. This clearly shows that sandwich molecules adsorb to the graphite surface by one of the phthalocyanine disks and its eight alkoxy groups. Despite the very similar mode of interaction with the surface, mixtures of alkoxylated (bisphthalocyaninato)erbium(III) with its (phthalocyaninato)cobalt(II)analogueshow partial phase separation on the nanoscale: areas are enriched in one of the compounds. A much clearer phase separation between (bisphthalocyaninato)erbium(III) and (phthalocyaninato)cobalt(II) molecules was achieved by mixing molecules containing alkoxy groups of different length. The results provide insight for the development of well-ordered nanostructures of bisphthalocyanines in the presence of phthalocyanines, which could be of importance for future nanometer-scale functional materials.
机译:镧系双酞菁配合物由于其独特的半导体和电致变色特性以及其双层结构,是构建二维(2D)有序阵列的有趣对象,有望在分子电子学中得到应用。通过扫描隧道显微镜研究了十二烷氧基取代的(双酞菁基)er(III)在固体(高度取向的热解石墨)-液体界面的二维自组装。结果表明,双酞菁分子形成有序的二维二维晶格(alpha = b = 3.0 +/- 0。+ /-1 nm,γ= 3度),几乎与其由(酞菁钴)钴形成的晶格相同( H)具有相同长度的类似物带有烷氧基链。这清楚地表明,夹心分子通过酞菁盘之一及其八个烷氧基吸附到石墨表面。尽管与表面的相互作用方式非常相似,但烷氧基化的(双酞菁基)er(III)与(酞菁基)钴(II)的混合物在纳米级上表现出部分相分离:区域富含一种化合物。通过混合含有不同长度烷氧基的分子,可以使(双酞菁基)er(Ⅲ)和(酞菁基)钴(Ⅱ)之间的相分离更加清晰。该结果为在存在酞菁的情况下开发有序的双酞菁纳米结构提供了见识,这对于将来的纳米级功能材料可能是重要的。

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