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Страница 1 от 36 резултата
Cooperative Conical Intersection Dynamics of Two Pyrazine Molecules in an Optical Cavity
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Hybrid light-matter states in optical cavities, known as polaritons, offer a novel means of manipulating and controlling photochemical processes. We investigate the cooperative cavity photochemistry of two pyrazine molecules undergoing conical intersection dynamics and interacting with a single
[Changes of microflora of the oral cavity after treatment with 2-sulfanilamido-3-methoxy-pyrazine (Kelfizin)].
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Closed-pore crystal capable of adsorbing CO2 onto isolated cavities generated by disorderly mixing of substituents on host skeleton.
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A single crystal adsorbent, [Rh(II)(2)(bza)(4)(2,3-empyz)](n) (2,3-empyz = 2-ethyl-3-methylpyrazine) (1), was synthesized by self-assembly reaction of a Rh(2) benzoate complex and substituted pyrazine linker. The compound consists of one-dimensional zigzag chains, which generated a closed-pore
Novel self-assembled supramolecular architectures of Mn(II) ions with a hybrid pyrazine-bipyridine ligand.
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A new hybrid pyrazine-bipyridine ligand L (C26H20N6) and its complexes with Mn(NO3)2, Mn(ClO4)2, MnCl2 and MnBr2 have been synthesised. By the self-assembly of L and Mn(II) ions three different kinds of supramolecular complexes have been obtained: binuclear baguette complex [Mn2L(H2O)6](NO3)4·2.5H2O
Crystal structure of di-aqua-bis-(2,6-di-methyl-pyrazine-κN (4))bis-(thio-cyanato-κN)cobalt(II) 2,5-di-methyl-pyrazine monosolvate.
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In the crystal structure of the title compound, [Co(NCS)2(C6H8N2)2(H2O)2]·C6H8N2, the Co(II) cation is coordinated by the N atoms of two terminal thio-cyanate anions, the O atoms of two water mol-ecules and two N atoms of two 2,6-di-methyl-pyrazine ligands. The coordination sphere of the resulting
Crystal structure of di-aqua-bis-(2,6-di-methyl-pyrazine-κN)bis-(thio-cyanato-κN)cobalt(II) 2,5-di-methyl-pyrazine tris-olvate.
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In the crystal structure of the title compound, [Co(NCS)2(C6H8N2)2(H2O)2]·3C6H8N2, the Co(II) cation is coordinated by two terminally N-bound thio-cyanate anions, two water mol-ecules and two 2,6-di-methyl-pyrazine ligands, forming a discrete complex with a slightly distorted octa-hedral N4O2
Pyrazine motif containing hexagonal macrocycles: synthesis, characterization, and host-guest chemistry with nitro aromatics.
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The synthesis and characterization of cationic two-dimensional metallamacrocycles having a hexagonal shape and cavity are described. Both macrocycles utilize a pyrazine motif containing an organometallic acceptor tecton with platinum(II) centers along with different donor ligands. While one
Structural diversity in coordination self-assembled networks of a multimodal ligand azacalix[4]pyrazine.
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We report herein the synthesis of a new heteracalixaromatic compound, tetramethylazacalix[4]pyrazine (TAPz), and its coordination self-assemblies with metal and metal cluster centers. Structural characterization of TAPz has shown that its conformation is fluxional in solution but exhibits a dominant
Conformational behavior of pyrazine-bridged and mixed-bridged cavitands: a general model for solvent effects on thermal "vase-kite" switching.
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The controllable switching of suitably bridged resorcin[4]arene cavitands between a "vase" conformation, with a cavity capable of guest inclusion, and a "kite" conformation, featuring an extended flattened surface, provides the basis for ongoing developments of dynamic molecular receptors, sensors,
Crystal structure of tri-aqua-(2,6-di-methyl-pyrazine-κN (4))bis-(thio-cyanato-κN)manganese(II) 2,5-di-methyl-pyrazine disolvate.
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In the crystal structure of the title complex, [Mn(NCS)2(C6H8N2)(H2O)3]·2C6H8N2, the Mn(II) cation is coordinated by two terminally N-bonded thio-cyanate anions, three water mol-ecules and one 2,6-di-methyl-pyrazine ligand within a slightly distorted N3O3 octa-hedral geometry; the entire complex
Formation of a narrow chiral cavity in bis-copper(ii) complexes of ferrocenylmethyl-l-tyrosine and its interaction with achiral guests.
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Earlier we reported the tendency of ferrocenylmethyl substituted amino acids to organize around Cu(ii) in a C(2) symmetry. In this paper we have utilized this property to form a chiral cavity using a l-tyrosine derivative. Structural characterization of [Cu(II)(S-fTyr)(2)(MeCN)(2)] (), where
Modifying the Nonradiative Decay Dynamics through Conical Intersections via Collective Coupling to a Cavity Mode.
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The coupling of a molecular ensemble to the confined electromagnetic modes of a microcavity can strongly modify the photophysics and photochemistry of the molecules upon photoexcitation. We investigate here how collective coupling effects lead to modifications of the mechanisms and rates of
A Host-Guest Supercapacitor Electrode Material Based on a Mixed Hexa-Transition Metal Sandwiched Arsenotungstate Chain and Three-Dimensional Supramolecular Metal-Organic Networks with One-Dimensional Cavities.
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The mixed hexa-transition metal (hexa-TM) sandwiched arsenotungstate derivative,
Alcohol-vapor inclusion in single-crystal adsorbents [M(II)2(bza)4(pyz)]n (M = Rh, Cu): structural study and application to separation membranes.
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The vapor absorbency of the series of alcohols methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol was characterized on the single-crystal adsorbents [M(II)2(bza)4(pyz)]n (bza = benzoate, pyz = pyrazine, M = Rh (1), Cu (2)). The crystal structures of all the alcohol inclusions were determined
Synthesis, Molecular Structure and Cytotoxicity of Molecular Materials Based on Water Soluble Half-Sandwich Rh(III) and Ir(III) Tetranuclear Metalla-Cycles.
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The neutral dinuclear complexes [(η⁵-C₅Me₅)₂Rh₂(μ-dhnq)Cl₂] (1) and [(η⁵-C₅Me₅)₂Ir₂(μ-dhnq)Cl₂] (2) (dhnqH₂ = 5,8-dihydroxy-1,4-naphthoquinone) were obtained from the reaction of [(η⁵-C₅Me₅)M(μ-Cl)Cl]₂ (M = Rh, Ir) with dhnqH₂ in the presence of CH₃COONa. Treatment of 1 or 2 in methanol with linear
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