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benzoquinone/zahnkaries
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Seite 1 von 26 Ergebnisse
Counter-ion modulation of long-distance pi-bonding of the open-shell p-benzoquinone anions.
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X-Ray crystallography of dichlorodicyano- or tetrachloro-p-benzoquinone salts with polyether-ligated alkali metals reveals discrete supramolecular complexes: [{M(L)A}(2)]. They show pairs of co-facial p-benzoquinone anions (A(-)) arranged at close interplanar separation: r(pi) approximately 2.9 A
Alkane-Shape-Selective Vapochromic Behavior Based on Crystal-State Host-Guest Complexation of Pillar[5]arene Containing One Benzoquinone Unit.
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Colored crystals of pillar[5]arene containing one benzoquinone unit were found to exhibit alkane-shape-selective vapochromic behavior. Activated pillar[5]arene crystals, prepared by removing solvated methanol from pillar[5]arene crystals, changed color from dark-brown to light-red after exposure to
A new supramolecular system of racemic-bis-beta-naphthol, benzoquinone and aromatic hydrocarbon, which shows high molecular recognition ability.
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Racemic-bis-beta-naphthol, benzoquinone and aromatic hydrocarbons formed a new three component supramolecular system as black crystals. X-ray analysis of the crystals shows that (+)- and (-)-bis-beta-naphthol and benzoquinone form a quinhydrone-type crystalline lattice with aromatic stacking and
Proximal cavity, distal histidine, and substrate hydrogen-bonding mutations modulate the activity of Amphitrite ornata dehaloperoxidase.
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Dehaloperoxidase (DHP) from Amphitrite ornata is the first globin that has peroxidase activity that approaches that of heme peroxidases. The substrates 2,4,6-tribromophenol (TBP) and 2,4,6-trichlorophenol are oxidatively dehalogenated by DHP to form 2,6-dibromo-1,4-benzoquinone and
Reduction of 1,4-quinone and ubiquinones by hydrogen atom transfer under UVA irradiation.
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1,4-Benzoquinone, coenzyme Q0 and Q10 were reacted with a series of hydrogen donors in the ESR cavity in the presence or absence of UVA irradiation. The signals of the radicals generated from the hydrogen donors or of those of the semiquinones were detected. The reaction mechanism was interpreted by
Overview of synthesis and structure of calix[n]quinone (n = 4, 6, 8)
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Calix[n]quinones, a class of cyclic oligomers composed of p-benzoquinone structures connected by methylene, have multi-conjugated carbonyl structures and adjustable cavities, which make their synthesis extremely attractive. In this minireview, thesynthetic methods of calix[n]quinones and the recent
A new method of solvation analysis: applications to quinones.
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A new method of analysis of the factor contributing to solvation of small molecules is described. Approximations of the energetic contributions to the entry of a molecule into water have been derived from partition coefficient data of solutes and selected derivatives from a multiplicity of solvents.
Expanded N-Confused Phlorin: A Platform for a Multiply Fused Polycyclic Ring System via Oxidation within the Macrocycle
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Novel interrupted π-conjugated macrocycles derived from expanded porphyrinoids were synthesized, and their unique reactivity was investigated in this work. The specific porphyrin analogs, so-called phlorins and isoporphyrins, possess a meso-sp3 methylene moiety, showing inner 3NH
The photochemistry of 4-chlorophenol in water revisited: the effect of cyclodextrins on cation and carbene reactions.
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The photochemistry of 4-chlorophenol (1) in water and in the presence of cyclodextrins has been studied by means of steady-state and time-resolved experiments. These have shown that 1 undergoes photoheterolysis of the C--Cl bond in the triplet state to yield the 4-hydroxyphenyl cation (3)2 in
Rendering the inedible edible: circumvention of a millipede's chemical defense by a predaceous beetle larva.
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The larva of the phengodid beetle, Phengodes laticollis, feeds on the millipede, Floridobolus penneri, without risking exposure to the repellent benzoquinones ordinarily ejected by the millipede from its defensive glands when attacked. The phengodid subdues the millipede by piercing the millipede's
Integration of homogeneous and heterogeneous advanced oxidation processes: Confined iron dancing with cyclodextrin polymer.
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A novel catalyst which integrates heterogeneous and homogenous Fenton reactions is designed and fabricated by encapsulating 2,5-dihydroxy-1,4-benzoquinone (2,5-DBQ) in ECDP-Fe3O4, a composite of Fe3O4 nanoparticles immobilized on a β-cyclodextrin polymer
Formal redox potentials of organic molecules in ionic liquids on the basis of quaternary nitrogen cations as adiabatic electron affinities.
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Formal redox potentials E°' involving neutral species R and radical anions R(•-) in ionic liquids (ILs) composed of ammonium, pyridinium, and imidazolium cations are discussed from the point of view of the adiabatic electron affinity as a molecular property. The dependence of the 1,4-benzoquinone
Self-assembled arene-ruthenium-based rectangles for the selective sensing of multi-carboxylate anions.
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Novel arene-ruthenium [2+2] metalla-rectangles 4 and 5 have been synthesized by self-assembly using dipyridyl amide ligand 3 and arene-ruthenium acceptors (arene: benzoquinone (1), naphthacenedione (2)) and characterized by NMR spectroscopy and ESI-MS. The solid-state structure of 5 was determined
Dynamic molecular tweezers composed of dibenzocyclooctatetraene units: synthesis, properties, and thermochromism in host-guest complexes.
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Novel dynamic molecular tweezers (DMTs) 3 a, 3 b, 4 a, 4 b, and 5 b, composed of two tub-shaped dibenzocyclooctatetraene (DBCOT) units, were designed and synthesized. The cyclooctatetraene (COT) rings of these DMTs readily invert in solution, and the molecular structure shows rigid syn and anti
Role of polarity of the distal pocket in the control of inhibitor binding in dehaloperoxidase-hemoglobin.
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Dehaloperoxidase (DHP A), a unique multifunctional enzyme, from the marine annelid Amphitrite ornata dehalogenates 2,4,6-tribromophenol to form 2,6-dibromo-1,4-benzoquinone. The catalytic cycle of DHP is similar to that of horseradish peroxidase (HRP), involving a high-valent ferryl heme and two
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