Molecular calixarene

The synergistic reaction of synergistic reaction CD with the subject recognition molecular — calixarene and crown ether... 

Progress in molecular recognition of functionalized calixarenes with hetero-atomic bridges as synthetic receptors 99MI43. 

Calixarenes including heterocyclic fragments as a rich source for molecular receptors 97G637. 

Based on the above results they have concluded that the ligand groups circularly arranged on the lower rim of the calixarene cavity construct a novel cyclic metal receptor for selective extraction of transition metal cations. Results suggest that the fine tuning in molecular... 

In a study of mixed monolayers of C60 and p-iert-butylcalix[8]arene, different isotherm behavior was obtained [256]. The surface pressure was observed to rise at a lower molecular area (1.00 nm molecule vs. 2.30 mn molecule in the prior study). Similar isotherms were observed whether a 1 1 mixture or a solution prepared by dissolving the preformed 1 1 complex was spread. The UV spectra of the transferred LB films appeared different than that of bulk C60. It was concluded that a stable 1 1 complex could be formed by spreading the solution either of the mixture or of the complex. This was confirmed in a later study by the same group that included separate spreading of the calixarene and the C60... 

Calixarenes, which are macrocyclic compounds, are one of the best building blocks to design molecular hosts in supramolecular chemistry [158]. Synthesis of calix[4]arenes, which have been adamantylated, has been reported [105, 109]. In calix[4]arenes, adamantane or its ester/carboxylic acid derivatives were introduced as substituents (Fig. 29). The purpose of this synthesis was to learn how to employ the flexible chemistry of adamantane in order to construct different kinds of molecular hosts. The X-ray structure analysis of p-(l-adamantyl)thiacalix[4]arene [109] demonstrated that it contained four CHCI3 molecules, one of which was located inside the host molecule cavity, and the host molecule assumed the cone-like conformational shape (Fig. 30). 

Liu, Y. Zhao, B. T. Wang, H. Chen, Q. F. Zhang, H. Y. Molecular design of calixarene 5. Syntheses and cation selectivities of novel Schiffs base p-tert-butylcalix-4-arenes. Chin. J. Chem. 2001, 19, 291-295. 

Heteroaryl groups are present in the 4-pyridyl-ethynyl compounds81,99,100 and their extended variants with C=C-C6H4-C=C-pyr-4 ligands.81,99 These compounds can be quaternized with Mel or coordinated to a metal complex at their terminal pyridyl functions to give species addressed as molecular rods or molecular wires.81,99 Similar reactions were carried out with 3-phenanthrolinyl-ethynyl complexes,62 and special examples are also known with R based on calixarenes.51... 

Metalated container molecules can be viewed as a class of compounds that have one or more active metal coordination sites anchored within or next to a molecular cavity (Fig. 2). A range of host systems is capable of forming such structures. The majority of these compounds represent macrocyclic molecules and steri-cally demanding tripod ligands, as for instance calixarenes (42), cyclodextrins (43,44), and trispyrazolylborates (45-48), respectively. In the following, selected types of metalated container molecules and their properties are briefly discussed and where appropriate the foundation papers from relevant earlier work are included. Porphyrin-based hosts and coordination cages with encapsulated metal complexes have been reviewed previously (49-53) and, therefore, only the most recent examples will be described. Thereafter, our work in this field is reported. 

Recently, it has been found that the outcome of some cycloadditions can be altered remarkably when performed inside the cavity of cyclodextrins (288), self-assembled molecular capsules (289), or coordination cages (290). This fact intrigued us greatly and stimulated our interest in the Diels-Alder reactivity of the calixarene-like [M2(L19)(L )]+ complexes bearing unsaturated carboxylate coligands L (215). 

C. A. Schalley, R, K. Castellano, M. S. Brody, D. M. Rudkevich, G. Siuzdak, J. Rebek, Jr, Investigating Molecular Recognition by Mass Spectrometry Characterization of Calixarene-Based Self-Assembling Capsule Hosts with Charged Guests , J. Am. Chern Soc, 1999, 121, 4568-4579. 

The network structures to be discussed will all involved hydrogen bonding as the supramolecular synthon. It should be noted however that other interactions such as coordinate bonds and host-guest interactions may also organise host molecules into network structures. Coordination polymers constructed from molecular hosts may involve functionalised calixarenes [8-11], cyclotriveratrylene [12], or cucurbituril [13]. Calixarenes have also been used to build up network structures via host-guest interactions [14,15]. It is also notable that volatile species may be trapped within the solid state lattice of calix[4] arene with a structure entirely composed of van der Waals interactions [16]. 

Box 10.2 Calixarene-based fluorescent molecular sensors for sodium ions... 

Among several families of compounds used as molecular models for such surface silanolic grafting sites (mono or poly-silanols [10-12], heteropolyanions [13, 14], calixarenes [15, 16], tripodal amido complexes [17], etc.) some silsesquioxanes [18-23] can be considered among the most convincing molecular analogues of silica surface silanols. 

In recent progress, calixarene resists have been prominent [105]. Hexaacetate p-methylcalix[6]arene was demonstrated to work as a high-resolution negative resist. This resist also shows high etch resistance. Calixarene resist has an advantage in its molecular size (about 1 nm). Liquid crystal resists and inorganic resists show high resolution [106]. These resists are suitable for the fabrication of nanostructures. However, the resist sensitivities are lower than those of chemically amplified resists, even PMMA. 

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