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Cristina García‐Simón Marc Garcia‐Borràs Dr. Laura Gómez Dr. Isaac Garcia‐Bosch Dr. Sílvia Osuna Prof. Marcel Swart Dr. Josep M. Luis Prof. Concepció Rovira Prof. Manuel Almeida Dr. Inhar Imaz Prof. Daniel Maspoch Dr. Miquel Costas Dr. Xavi Ribas 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(4):1445-1456
The metal‐directed supramolecular synthetic approach has paved the way for the development of functional nanosized molecules. In this work, we report the preparation of the new nanocapsule 3? (CF3SO3)8 with a A4B2 tetragonal prismatic geometry, where A corresponds to the dipalladium hexaazamacrocyclic complex Pd‐1 , and B corresponds to the tetraanionic form of palladium 5,10,15,20‐tetrakis(4‐carboxyphenyl)porphyrin ( 2 ). The large void space of the inner cavity and the supramolecular affinity for guest molecules towards porphyrin‐based hosts converts this nanoscale molecular 3D structure into a good candidate for host–guest chemistry. The interaction between this nanocage and different guest molecules has been studied by means of NMR, UV/Vis, ESI‐MS, and DOSY experiments, from which highly selective molecular recognition has been found for anionic, planar‐shaped π guests with association constants (Ka) higher than 109 M ?1, in front of non‐interacting aromatic neutral or cationic substrates. DFT theoretical calculations provided insights to further understand this strong interaction. Nanocage 3? (CF3SO3)8 can not only strongly host one single molecule of M(dithiolene)2 complexes (M=Au, Pt, Pd, and Ni), but also can finely tune their optical and redox properties. The very simple synthesis of both the supramolecular cage and the building blocks represents a step forward for the development of polyfunctional supramolecular nanovessels, which offer multiple applications as sensors or nanoreactors. 相似文献
244.
Dr. Luca Gabrielli Dr. Laura Russo Dr. Ana Poveda Dr. Julian R. Jones Prof. Francesco Nicotra Dr. Jesús Jiménez‐Barbero Prof. Laura Cipolla 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(24):7856-7864
Hybrid organic–inorganic solids represent an important class of engineering materials, usually prepared by sol–gel processes by cross‐reaction between organic and inorganic precursors. The choice of the two components and control of the reaction conditions (especially pH value) allow the synthesis of hybrid materials with novel properties and functionalities. 3‐Glycidoxypropyltrimethoxysilane (GPTMS) is one of the most commonly used organic silanes for hybrid‐material fabrication. Herein, the reactivity of GPTMS in water at different pH values (pH 2–11) was deeply investigated for the first time by solution‐state multinuclear NMR spectroscopic and mass spectrometric analysis. The extent of the different and competing reactions that take place as a function of the pH value was elucidated. The NMR spectroscopic and mass spectrometric data clearly indicate that the pH value determines the kinetics of epoxide hydrolysis versus silicon condensation. Under slighly acidic conditions, the epoxy‐ring hydrolysis is kinetically more favourable than the formation of the silica network. In contrast, under basic conditions, silicon condensation is the main reaction that takes place. Full characterisation of the formed intermediates was carried out by using NMR spectroscopic and mass spectrometric analysis. These results indicate that strict control of the pH values allows tuning of the reactivity of the organic and inorganic moities, thus laying the foundations for the design and synthesis of sol–gel hybrid biomaterials with tuneable properties. 相似文献
245.
Alternating copolymers of vinyl acetate (VAc) and maleic anhydride (MA) are produced preferentially when VAc and MA are copolymerized at moderate temperatures while random copolymers are produced at temperatures above 90°C. A charge-transfer complex (CTC) of VAc/MA exists at moderate temperatures but does not exist at temperatures above 90°C. 相似文献
246.
Edward N. Peters 《高分子科学杂志,C辑:聚合物评论》2013,53(2):173-208
The need for elastomeric polymers which will maintain their elastic properties at high temperatures has led to a wide interest in inorganic-based polymers [l]. The development of carborane-siloxane polymers in the early 1960s was a breakthrough in the search for a high-temperature elastomer. Incorporation of a carborane moiety into the siloxane backbone significantly enhanced the overall thermal stability [2]. 相似文献
247.
We describe an approach using ring‐closing metathesis (RCM) to synthesize versatile coumarin derivatives that present appropriate substitutions both at the aromatic and at the α,β‐unsaturated lactone ring. The obtained compounds can be used as molecular scaffolds suitable for further diversifications through a combinatorial approach. 相似文献
248.
Dr. Awal Noor Tobias Bauer Dr. Tanya K. Todorova Prof. Dr. Birgit Weber Prof. Dr. Laura Gagliardi Prof. Dr. Rhett Kempe 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(30):9825-9832
Herein, the ligand‐based concept of shortening quintuple bonds and some of its limitations are reported. In dichromium–diguanidinato complexes, the length of the quintuple bond can be influenced by the substituent at the central carbon atom of the used ligand. The guanidinato ligand with a 2,6‐dimethylpiperidine backbone was found to be the optimal ligand. The reduction of its chromium(II) chloride–ate complex gave a quintuply bonded bimetallic complex with a Cr? Cr distance of 1.7056 (12) Å. Its metal–metal distance, the shortest observed in any stable compound yet, is of essentially the same length as that of the longest alkane C? C bond (1.704 (4) Å). Both molecules, the alkane and the Cr complex, are of remarkable stability. Furthermore, an unsupported CrI dimer with an effective bond order (EBO) of 1.25 between the two metal atoms, indicated by CASSCF/CASPT2 calculations, was isolated as a by‐product. The formation of this by‐product indicates that with a certain bulk of the guanidinato ligand, other coordination isomers become relevant. Over‐reduction takes place, and a chromium–arene sandwich complex structurally related to the classic dibenzene chromium complex was observed, even when bulkier substituents are introduced at the central carbon atom of the used guanidinato ligand. 相似文献
249.
Georgina Fortuny Laura Pineda Antoni Rúbies Francesc Centrich Ramon Companyó 《International journal of environmental analytical chemistry》2013,93(7):707-726
A method for determination of 61 organic pollutants (polycyclic aromatic hydrocarbons and organochlorine, organophosphorous and organonitrogen pesticides) is proposed. It is based on solid phase extraction (SPE) and subsequent analysis of the extract by liquid and gas chromatography coupled to tandem mass spectrometry. Method validation yielded to the following values: limits of quantification, from 0.005 to 0.020?µg?L?1; trueness, 95% to 113% and reproducibility (as percent relative standard deviation), 2% to 15%. Additionally, the method performed well in various proficiency tests. 相似文献
250.
Maria G. Bettoli Lorenzo Cantelli Damiano Quarin Marzia Ravanelli Laura Tositti Ottavio Tubertini 《International journal of environmental analytical chemistry》2013,93(3-4):321-330
Abstract 210Pb is widely used to determine accumulation rates in order to obtain a time scale in environmental samples. The most accurate method uses the determination of 210Pb via its grand-daughter 210Po by alpha spectrometry. Unfortunately this method requires a complex wet-chemistry procedure to achieve the separation of 210Po from its matrix. In this work a simplified procedure for the chemical separation of 210Po is proposed and applied to three marine sediment cores and a 10 m snow core collected in Antarctica. The calculated sedimentation rates for marine sediments range from 0.053 to 0.071 cm y?1. The mean annual accumulation rate for the snow is 16.6 cm y?1 w.e. A comparison with literature data in the same region is given. 相似文献