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Leht 1 alates 16 tulemused
Convergent synthesis of alternating fluorene-p-xylene oligomers and delineation of the (silver) cation-induced folding.
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Convergent synthetic routes for the preparation of hitherto unknown fluorene-p-xylene oligomers (containing up to 10 fluorene moieties) from readily available starting materials are described. The conformationally adaptable monomeric receptor (which is made of a pair of fluorene and one p-xylene
Controlling the spatial orientation of molecular actuators: polarized photoisomerization of 2-nitro-9-(2,2,2-triphenylethylidene)fluorene in a thin polymer matrix.
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The molecule 2-nitro-9-(2,2,2-triphenylethylidene)fluorene (NTEF) was studied as a potential light-driven molecular motor. Absorption at 355 nm causes a reversible spatial reorientation of the angular distribution of the dibenzofulvene rotor moiety of NTEF when immobilized in a poly(methyl
Room-temperature lasing from fluorene thin-film crystals densely doped with anthracene.
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The potential for room-temperature lasing in densely doped organic crystals has been examined using (fluorene)0.8-(anthracene)0.2 thin crystals fabricated in a narrow gap between two quartz plates. An excitation-intensity dependence study confirms that the system shows spectral line narrowing, a
Solvent mediated intramolecular photoinduced electron transfer in a fluorene-perylene bisimide derivative.
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Photoinduced electron transfer from fluorene to perylene bisimide has been studied for 2,7-bis(N-(1-hexylheptyl)-3,4:9,10-perylene-bisimide-N'-yl))-9,9-didodecylfluorene (PFP) in 11 different organic solvents. The intramolecular charge-separated state in PFP is almost isoenergetic with the locally
Tunable fluorescence behaviors of a supramolecular system based on a fluorene derivative and cucurbit[8]uril and its application for ATP sensing.
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In this work, we developed a supramolecular fluorescent system based on host-guest interactions between a fluorene derivative carrying two bispyridinium units (FPy) and cucurbit[8]uril (CB[8]). In aqueous solution, the system showed outstanding tunable emission properties. After being encapsulated
Lasing in organic mixed-crystal thin films with cavities composed of naturally formed cracks.
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This study investigates the possibility that a crack pair that is naturally formed in the course of sample preparation functions as a laser cavity. Lasing with longitudinal mode structures has been reported in mixed-crystal thin films composed of fluorene and anthracene without artificial cavity
Solution-Crystallization and Related Phenomena in 9,9-Dialkyl-Fluorene Polymers. I. Crystalline Polymer-Solvent Compound Formation for Poly(9,9-dioctylfluorene).
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Polymer-solvent compound formation, occurring via co-crystallization of polymer chains and selected small-molecular species, is demonstrated for the conjugated polymer poly(9,9-dioctylfluorene) (PFO) and a range of organic solvents. The resulting crystallization and gelation processes in PFO
Identification of novel Nicotinamide Phosphoribosyltransferase (NAMPT) inhibitors using computational approaches.
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Nicotinamide Phosphoribosyltransferase (NAMPT) is a rate-limiting enzyme in the biosynthesis of NAD. Cancer cells have elevated poly [ADP-Ribose] polymerase 1 (PARP) activity as well as the immense necessity of ATP: thereby consuming NAD at a higher rate than normal tissues. The perturbation of
Rearrangement of meta-Bridged Calix[4]arenes Promoted by Internal Strain.
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The meta-bridged calixarenes possess a rigidified and highly distorted cavity, where the additional single-bond bridge imposes an extreme internal strain on the whole system. As a consequence, these compounds exhibit a reasonably amended reactivity, compared with common calix[4]arene derivatives,
Silver(I) compounds consisting of [2.2]paracyclophane: reversible guest-driven solid-state transformation and incorporation behavior.
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Reaction of [2.2]paracyclophane with silver(I) heptafluorobutyrate (AgC3F7CO2) has isolated three novel networks: [Ag4(pcp)(C3F7CO2)4] x pyrene (1), [Ag4(pcp)(C3F7CO2)4] x phen (phen = phenanthrene) (2), and [Ag4(pcp)(C3F7CO2)4] x fluorene (3), and an intercalation compound [Ag4(pcp)(C3F7CO2)4] x
Nanophase separation in polystyrene-polyfluorene block copolymers thin films prepared through the breath figure procedure.
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The amphiphilic block copolymer formed by a hydrophobic body of polystyrene and a hydrophilic head of poly[9,9-di(2-(2-tetrahydropyranyl-oxy)hexyl)fluorene-alt-9,9-dioctylfluorene] was synthesized, and its solution was used to create thin films with ordered pattern of holes, by means of the breath
Photomagnetic properties in a series of spin crossover compounds
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The spin crossover (SC) compounds [Fe(PM-AzA)2(NCX)2] and [Fe(PM-FIA)2(NCX)2] (with PM-AzA = N-2'-pyridylmethylene-4-(phe-nylazo)aniline, PM-FIA = N-2'-pyridylmethylene-4-(2-amino)fluorene, and X = S, Se) have been prepared. The SC regimes have been deduced from variable-temperature magnetic
Metalla-Assembled Electron-Rich Tweezers: Original Redox-Controlled Guest Release through Supramolecular Dimerization.
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Developing methodologies to control on demand the release of a molecular guest requires the rational design of stimuli-responsive hosts bearing functional cavities. While a substantial number of responsive metalla-cages have been described so far, the case of coordination-tweezers has been less
Homology modeling, simulation and molecular docking studies of catechol-2, 3-Dioxygenase from Burkholderia cepacia: Involved in degradation of Petroleum hydrocarbons.
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Catechol 2, 3-dioxygenase is present in several types of bacteria and undergoes degradation of environmental pollutants through an important key biochemical pathways. Specifically, this enzyme cleaves aromatic rings of several environmental pollutants such as toluene, xylene, naphthalene and
Enhanced solubilisation of six PAHs by three synthetic cyclodextrins for remediation applications: molecular modelling of the inclusion complexes.
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Solubilisation of six polycyclic aromatic hydrocarbons (PAHs) (acenaphthene, anthracene, fluoranthene, fluorene, phenanthrene and pyrene) by three synthetic cyclodextrins (CDs) (2-hydroxypropyl-β-CD, hydroxypropyl-γ-CD and randomly methylated-β-CD) was investigated in order to select the CD which
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