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341.
Bonnet S Siegler MA Costa JS Molnár G Bousseksou A Spek AL Gamez P Reedijk J 《Chemical communications (Cambridge, England)》2008,(43):5619-5621
The two-step spin crossover of a new mononuclear iron(ii) complex is studied by magnetic, crystallographic and calorimetric methods revealing two successive first-order phase transitions and an ordered intermediate phase built by the repetition of the unprecedented [HS-LS-LS] motif. 相似文献
342.
Steinhaus graphs on vertices are certain simple graphs in bijective correspondence with binary -sequences of length . A conjecture of Dymacek in 1979 states that the only nontrivial regular Steinhaus graphs are those corresponding to the periodic binary sequences of any length . By an exhaustive search the conjecture was known to hold up to 25 vertices. We report here that it remains true up to 117 vertices. This is achieved by considering the weaker notion of parity-regular Steinhaus graphs, where all vertex degrees have the same parity. We show that these graphs can be parametrized by an -vector space of dimension approximately and thus constitute an efficiently describable domain where true regular Steinhaus graphs can be searched by computer.
343.
Polystyrene nanoparticles doped with a luminescent europium complex, Eu(tta)(3)phen, are prepared by miniemulsion polymerization. The influence of the complex on the miniemulsion polymerization is investigated by the systematic variation of the initial concentration of Eu(tta)(3)phen from 2 to 7 wt% relatively to styrene. A maximum doping level of about 2% by weight in the final particles can be achieved. At higher doping levels, destabilization of the miniemulsion leads to a loss of reproducibility with respect to both the degree of conversion and the final Eu content of the particles. Doped nanoparticles of varying diameter, ranging from 19 to 94 nm, are successfully prepared. Steady-state and time-resolved luminescence measurements indicate that the luminescence properties of Eu(tta)(3)phen in the doped latexes are unchanged from those found in THF solution. Aqueous dispersions of the doped particles exhibit characteristic red emission under UV light irradiation. The luminescence intensity increases linearly with Eu(tta)(3)phen content, indicating the absence of self-quenching despite the relatively high local concentrations within the particles. 相似文献
344.
Levine DR Caruso A Siegler MA Tovar JD 《Chemical communications (Cambridge, England)》2012,48(50):6256-6258
The synthesis of new boron-containing acenes (meta-B-entacenes) is reported. These compounds exhibit slightly non-planar core geometries with blue-shifted spectral properties and more negative electrochemical reduction potentials relative to known para isomers. Polarizable π-extended architectures were realized via cross-coupling procedures with chloro-functionalized precursors. 相似文献
345.
Sanguinet L Pozzo JL Guillaume M Champagne B Castet F Ducasse L Maury E Soulié J Mançois F Adamietz F Rodriguez V 《The journal of physical chemistry. B》2006,110(22):10672-10682
This paper presents a series of acidoswitchable NLO-phores combining the 9-methylbenzimidazolo[2,3-b]oxazolidine core with various pi systems such as phenylethenyl, phenylethynyl, and naphthylethenyl. All the prepared derivatives are shown to display acidochromic behavior at ambient temperature. The remarkable contrast in the NLO response along the reversible transformations observed in HRS experiments is rationalized by high level theoretical calculations. 相似文献
346.
Trinuclear copper(II) complex [CuII3(NIT2PhO)2Cl4] was synthesized with p-cresol-substituted bis(α-nitronyl nitroxide) biradical: 4-methyl-2,6-bis(1-oxyl-3-oxido-4,4,5,5-tetramethyl-2-imidazolin-2-yl)phenol (NIT2PhOH). The crystal structure of this heterospin complex was determined using single-crystal X-ray diffraction analysis and exhibits four unusual seven-membered metallocycles formed from the coordination of oxygen atoms of the N-O groups and of bridging phenoxo (µ-PhO−) moieties with copper(II) ions. The crystal structure analysis reveals an incipient agostic interaction between a square planar copper center and a hydrogen-carbon bond from one methyl group carried on the coordinated nitronyl-nitroxide radical. The intramolecular Cu∙∙∙H-C interaction involves a six-membered metallocycle and may stabilize the copper center in square planar coordination mode. From the magnetic susceptibility measurements, the complex, which totals seven S = 1/2 spin carriers, has almost a ground state spin S = 1/2 at room temperature ascribed to strong antiferromagnetic interaction between the nitronyl nitroxide moieties and the copper(II) centers and in between the copper(II) centers through the bridging phenoxo oxygen atom. 相似文献
347.
Clment Kotras Maxime Leclercq Maxime Roger Camille Bouillon Antonio Recupido Aurlien Lebrun Yannick Bessin Philippe Gerbier Sbastien Richeter Sbastien Ulrich Sbastien Clment Mathieu Surin 《Molecules (Basel, Switzerland)》2022,27(19)
Dynamic covalent polymers (DCPs) offer opportunities as adaptive materials of particular interest for targeting, sensing and delivery of biological molecules. In this view, combining cationic units and fluorescent units along DCP chains is attractive for achieving optical probes for the recognition and delivery of nucleic acids. Here, we report on the design of acylhydrazone-based DCPs combining cationic arginine units with π-conjugated fluorescent moieties based on thiophene-ethynyl-fluorene cores. Two types of fluorescent building blocks bearing neutral or cationic side groups on the fluorene moiety are considered in order to assess the role of the number of cationic units on complexation with DNA. The (chir)optical properties of the building blocks, the DCPs, and their complexes with several types of DNA are explored, providing details on the formation of supramolecular complexes and on their stability in aqueous solutions. The DNA-templated formation of DCPs is demonstrated, which provides new perspectives on the assembly of fluorescent DCP based on the nucleic acid structure. 相似文献
348.
Kim Anh Nguyen Emilie Lesur Maxime Ribéraud Antoine Sallustrau Davide Audisio Frédéric Taran 《Helvetica chimica acta》2023,106(3):e202200187
The synthesis of four clickable sydnone-heptamethine cyanine derivatives is described in this article. The synthetic route is based on a palladium-cross coupling reactions of sydnone boronates affording the desired sydnone-cyanine conjugates in only five steps. These compounds were shown to react smoothly with cyclooctynes to form the corresponding pyrazoles clicked products quantitatively at room temperature and with rate constants up to 18 m −1 ⋅ s−1, affording interesting new tools for biorthogonal fluorescent labelling of (bio)molecules. Fluorescence properties of both sydnone- and pyrazole-cyanines are described, as well. 相似文献
349.
Alexandre Labiche Augustin Malandain Maxime Molins Dr. Frédéric Taran Dr. Davide Audisio 《Angewandte Chemie (International ed. in English)》2023,62(36):e202303535
In contrast to stable and natural abundant carbon-12, the synthesis of organic molecules with carbon (radio)isotopes must be conceived and optimized in order to navigate through the hurdles of radiochemical requirements, such as high costs of the starting materials, harsh conditions and radioactive waste generation. In addition, it must initiate from the small cohort of available C-labeled building blocks. For long time, multi-step approaches have represented the sole available patterns. On the other side, the development of chemical reactions based on the reversible cleavage of C−C bonds might offer new opportunities and reshape retrosynthetic analysis in radiosynthesis. This review aims to provide a short survey on the recently emerged carbon isotope exchange technologies that provide effective opportunity for late-stage labeling. At present, such strategies have relied on the use of primary and easily accessible radiolabeled C1-building blocks, such as carbon dioxide, carbon monoxide and cyanides, while the activation principles have been based on thermal, photocatalytic, metal-catalyzed and biocatalytic processes. 相似文献
350.
Maxime Robin Stephane Mialhe Valerie Pique Robert Faure Jean‐Pierre Galy 《ChemInform》2002,33(38):153-153