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首页> 外文期刊>Chemistry: A European journal >Liquid-phase epitaxy of multicomponent layer-based porous coordination polymer thin films of [M(L)(P)0.5] type: Importance of deposition sequence on the oriented growth
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Liquid-phase epitaxy of multicomponent layer-based porous coordination polymer thin films of [M(L)(P)0.5] type: Importance of deposition sequence on the oriented growth

机译:[M(L)(P)0.5]型多组分层多孔配位聚合物薄膜的液相外延:沉积顺序对定向生长的重要性

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The progressive liquid-phase layer-by-layer (LbL) growth of anisotropic multicomponent layer-based porous coordination polymers (PCPs) of the general formula [M(L)(P)0.5] (M: Cu2+, Zn2+; L: dicarboxylate linker; P: dinitrogen pillar ligand) was investigated by using either pyridyl- or carboxyl-terminated self-assembled monolayers (SAMs) on gold substrates as templates. It was found that the deposition of smooth, highly crystalline, and oriented multilayer films of these PCPs depends on the conditions at the early growth cycles. In the case of a two-step process with an equimolar mixture of L and P, growth along the [001] direction is strongly preferred. However, employing a three-step scheme with full separation of all components allows deposition along the [100] direction on carboxyl-terminated SAMs. Interestingly, the growth of additional layers on top of previously grown oriented seeding layers proved to be insensitive to the particular growth scheme and full retention of the initial orientation, either along the [001] or [100] direction, was observed. This homo- and heteroepitaxial LbL growth allows full control over the orientation and the layer sequence, including introduction of functionalized linkers and pillars. One layer at a time: The stepwise liquid-phase layer-by-layer growth of anisotropic, multicomponent layer-based porous coordination polymers (PCPs) of the general formula [M(L)(P) 0.5] (M: Cu2+, Zn2+; L: dicarboxylate linker, P: dinitrogen pillar ligand) was investigated by using either pyridyl- or carboxyl-terminated self-assembled monolayers as templates. Highly oriented PCP multilayers were selectively grown along the [100] and [001] directions (see figure).
机译:通式[M(L)(P)0.5](M:Cu2 +,Zn2 +; L:二羧酸盐)的基于各向异性多组分层的多孔配位聚合物(PCPs)的液相逐层(LbL)生长接头; P:二氮键配体)是通过在金底物上使用吡啶基或羧基封端的自组装单层(SAMs)进行研究的。已经发现,这些PCP的光滑,高度结晶和取向的多层膜的沉积取决于早期生长周期的条件。在采用L和P的等摩尔混合物的两步法的情况下,强烈优选沿[001]方向的生长。但是,采用三步方案,将所有组分完全分离,可以在羧基末端的SAM上沿[100]方向沉积。有趣的是,在先前生长的定向种子层之上的其他层的生长被证明对特定的生长方案不敏感,并且观察到了沿[001]或[100]方向的初始方向的完全保留。这种同质和异质外延LbL的生长可以完全控制方向和层序列,包括引入功能化的连接基和柱。一次一层:逐步多层液相生长各向异性[M(L)(P)0.5]的各向异性多组分层多孔配位聚合物(PCP)(M:Cu2 +,Zn2 + ; L:二羧酸酯连接基,P:二氮支柱配体)以吡啶基或羧基封端的自组装单层为模板进行了研究。高度定向的PCP多层沿着[100]和[001]方向选择性生长(见图)。

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