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Phenylephrine and (+/-)N-[5-(4,5-dihydro-1-H-imidazol-2yl)-2-hydroxy-5,6,7,8-tetr ahydronaphthalen-1-yl] methanesulphonamide hydrobromide (A 61603) evoked concentration-dependent contractions of the rabbit spleen. These contractions were antagonized by prazosin (10(-8)-10(-7) M) with pA2 values of 8.34+/-0.11 and 8.15+/-0.10 against phenylephrine and A 61603, respectively. In both cases, the slopes of the Schild plots were not significantly (P>0.05) different from 1.0, indicating competitive antagonism. The effects of subtype-selective antagonists WB 4101 [2-(2-6-dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane hydrochloride] and 5-methylurapidil on agonist-induced contractions were also examined. WB 4101 competitively antagonized agonist-induced contractions; pA2 values were 8.13+/-0.10 and 8.10+/-0.03 against phenylephrine and A 61603, respectively. Corresponding values for 5-methylurapidil were 8.28+/-0.17 and 7.93+/-0.02 against phenylephrine and A 61603, respectively. Tamsulosin and Rec 15/2739 [(8-3-[4-(2-methoxyphenyl)-1-piperazinyl]-propylcarbamoyl)-3-methy l-4-oxo-2-phenyl-4H-1-benzopyran dihydrochloride] also antagonized phenylephrine- and A 61603-induced contractions with pA2 values of 9.38+/-0.13 and 9.18+/-0.06 (tamsulosin) and 8.41+/-0.12 and 8.34+/-0.11 (Rec 15/2739) against phenylephrine and A 61603, respectively. HV 723 (alpha-ethyl-3,4,5-trimethoxy-alpha-(3-((2-(2-methoxyphenoxyethyl) -amino)-propyl)benzene-aceto-nitrile) fumarate) competitively antagonized phenylephrine-induced contractions with a pA2 value of 8.57+/-0.06. Chloroethylclonidine (CEC; 10(-4) M) shifted phenylephrine and A 61603 concentration-response curves to the right, reducing their potencies approximately two- to threefold, while the maximum response was reduced by 8% in both cases. It was therefore concluded that contractions of the rabbit spleen induced by alpha1-adrenergic agonists were mediated predominantly by a relatively CEC-insensitive alpha1-adrenoceptor subtype, possibly the alpha1L-subtype.
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PMID:Functional characterization of alpha1-adrenoceptor subtypes in the rabbit spleen. 977 16

Photochromic performance of diarylethene single crystals was controlled by crystal engineering using non-covalent aromatic-aromatic interactions as the directional intermolecular force. A diarylethene derivative with two pentafluorophenyl groups, 1,2-bis(2-methyl-5-pentafluorophenyl-3-thienyl)perfluorocyclopentene (1a), formed stoichiometric co-crystals with benzene (Bz) and naphthalene (Np) by aryl-perfluoroaryl interactions. Face-to-face pi-stacking interactions between the pentafluorophenyl groups of 1a and the aromatic molecules are responsible for 2:1 and 1:1 stoichiometric compositions in 1a/Bz and 1a/Np co-crystals, respectively. The diarylethene underwent thermally stable and photoreversible photochromic reactions in a homo-crystal of 1a and co-crystals 1a/Bz and 1a/Np. The absorption spectra of the photogenerated closed-ring isomers varied depending on the conformation of the diarylethene molecules packed in the crystals. The diarylethene 1a also formed 1:1 stoichiometric co-crystals with different kinds of diarylethenes, 1,2-bis(2-ethyl-5-phenyl-3-thienyl)perfluorocyclopentene (2a) and 1,2-bis[2-methyl-5-(1-naphthyl)-3-thienyl]perfluorocyclopentene (3a). Both co-crystals 1a/2a and 1a/3a showed photochromism. Although 1a, 2a, and 3a underwent efficient photocyclization reactions in their homo-crystals, highly selective photocyclization reactions of 2a or 3a were observed in the co-crystals. The selective reactions were confirmed by HPLC and X-ray crystallography. Excited energy transfers from 1a to 2a and from 1a to 3a are considered to occur and cause the selective reactions.
Chem Rec 2004
PMID:Crystal engineering of photochromic diarylethene single crystals. 1505 66

Rearrangement of a carbene/carbenoid intermediate to form an acetylene moiety, known as the Fritsch-Buttenberg-Wiechell (FBW) rearrangement, was developed for the formation of polyynes and polyyne frameworks within highly conjugated organic materials. Necessary precursors can be prepared through formation of an alkynyl ketone, followed by dibromoolefination under Corey-Fuchs conditions. The carbenoid rearrangement is brought about by treatment of the dibromoolefin with BuLi under mild conditions. The success of these FBW reactions is quite solvent-dependent, and nonpolar hydrocarbon solvents (e.g., hexanes, toluene, benzene) work quite well, while use of ethereal solvents such as diethyl ether and tetrahydrofuran (THF) does not provide the desired polyyne product. This protocol was successfully applied to the formation of silyl, alkyl, alkenyl, and aryl polyynes, including di-, tri-, and tetrayne products, as well as the construction of two-dimensional carbon-rich molecules. A one-pot variant of this procedure is being developed and is particularly applicable toward the synthesis of polyyne natural products. Formation of a series of triisopropylsilyl end-capped polyynes, from the triyne to decayne, was achieved. Third-order nonlinear optical properties of these polyynes were evaluated. This study shows that the molecular second hyperpolarizabilities for the polyynes as a function of length increase at a rate that is higher than all other nonaromatic organic oligomers.
Chem Rec 2006
PMID:Polyyne synthesis using carbene/carbenoid rearrangements. 1690 94

Self-assembly of metal ions and organic ligands results in the formation of extended or discrete metallosupramolecular structures. In case of neutral ditopic ligands such as bisterpyridines, extended metallosupramolecular coordination polyelectrolytes (MEPEs) are formed. Metal ion-induced self-assembly of 1,4-bis(2,2':6',2''-terpyridin-4'-yl)benzene with Fe(II) or Co(II) results in MEPEs with interesting electrochemical properties. These MEPEs reversibly change their color when oxidized or reduced. The heterometallic MEPE consisting of Fe(II) and Co(II) combines the properties of the individual MEPEs and therefore shows their different states: red-purple, blue, and transparent. On the other hand, complexation of cyclic phenylazomethines with metal ions results in discrete metallosupramolecular structures. We find that metal ion assembly to the organic module occurs in a stepwise fashion because of a difference in the basicity of the imine conformers, and the metal ion assembly can be controlled electrochemically. This example illustrates how metal ion binding can be controlled by the conformation of the receptor, an important step toward assembling organic ligands and metal ions in predictable ways.
Chem Rec 2007
PMID:Electrochemical functions of metallosupramolecular nanomaterials. 1766 46

L-glutamate is the major excitatory neurotransmitter in the mammalian central nervous system. Termination of glutamate receptor activation and maintenance of low extracellular glutamate concentrations are mainly achieved by glutamate transporters [excitatory amino acid transporters 1-5 (EAAT1-5)] located in nerve endings and surrounding glial cells. Selective and potent inhibitors have long been required to investigate the physiological significance of transporters in the regulation of synaptic transmission and the pathogenesis of neurological diseases. Non-transportable blockers are desirable because, unlike competitive substrates, they do not cause ion flux and heteroexchange. After a series of possible candidate molecules, we synthesized threo-beta-benzyloxyaspartate (TBOA), the first non-transportable blocker for all subtypes of EAATs. In addition, TBOA analogs with a bulky substituent on their benzene ring showed enhanced inhibition of labeled glutamate uptake. Comparing the effects of substrates and non-transportable blockers revealed the physiological roles of EAATs. We also developed a novel binding assay system using a tritium-labeled TBOA analog. In this review, we describe the design and synthesis of these blockers and the functions of the EAATs elucidated with them.
Chem Rec 2008
PMID:Glutamate transporter blockers for elucidation of the function of excitatory neurotransmission systems. 1856 34

Theoretical and computational methods are powerful in studying transition metal complexes. Our theoretical studies of C-H sigma-bond activation of benzene by Pd(II)-formate complex and that of methane by Ti(IV)-imido complex successfully disclosed that these reactions are understood to undergo heterolytic sigma-bond activation and the driving force is the formation of strong O-H and N-H bonds in the former and the latter, respectively. Orbital interactions are considerably different from those of sigma-bond activation by oxidative addition. The transmetallation, which is a key process in the cross-coupling reaction, is understood to be heterolytic sigma-bond activation. Our theoretical study clarified how to accelerate this transmetallation. Also, we wish to discuss weak points in theoretical and computational studies of large systems including transition metal elements, such as the necessity to incorporate solvation effect and to present quantitatively correct numerical results. The importance of solvation effects is discussed in the oxidative addition of methyliodide to Pt(II) complex which occurs in a way similar to an S(N)2 substitution. To apply the CCSD(T) (coupled cluster singles and doubles with perturbative triples correction) method, which is the gold standard of electronic structure theory, to large system, we need to reduce the size of the system by employing a small model. But, such modeling induces neglects of electronic and steric effects of substituents which are replaced in the small model. Frontier-orbital-consistent quantum-capping potential (FOC-QCP) was recently proposed by our group to incorporate the electronic effects of the substituents neglected in the modeling. The CCSD(T) calculation with the FOC-QCP was successfully applied to large systems including transition metal elements.
Chem Rec 2010 Mar
PMID:Theoretical and computational studies of organometallic reactions: successful or not? 2019 36

In this article, novel gel-forming materials based on oligomeric and polymeric electrolytes for not only water but also organic solvents, including ionic liquids, are highlighted especially the synthesis, derivatization, and physical property. The oligoelectrolytes with cationic pyridinium backbone can be very easily prepared by the intermolecular quaternization of the ampholytic monomer. The ionene polymers with N,N'-(p-phenylene)dibenzamide linkages as polyelectrolyte were also straightforwardly synthesized in high yields by the copolymerization of 1,4-bis[4-(chloromethyl)benzamide]benzene and commercially available alpha,omega-ditertiary amines. The oligo- and polyelectrolytes provided physical hydrogels under ca. 1-5 wt% of the concentrations after heating and cooling at room temperature without any other additives. These cationic gelators have characteristic properties, such as acid resistance, a self-healing nature after mechanical collapse, and a dispersant ability for single-walled carbon nanotubes, which have been rarely attainable for conventional physical gelators.
Chem Rec 2010 Aug
PMID:Ionic gelators: oligomeric and polymeric electrolytes as novel gel forming materials. 2060 62

Polymer-incarcerated metal(0) nanocluster catalysts were developed based on two techniques: microencapsulation and cross-linking. Pd, Au, Pt, and bimetallic nanoclusters could be efficiently immobilized on polymers containing benzene rings keeping subnanometer- to nanometer-size clusters. Catalysts could be used for redox reactions using molecular hydrogen and oxygen, and could be reused without aggregation of nanoclusters and leaching of metals. Modification of polymers and addition of second inorganic supports sometimes increased their reactivity.
Chem Rec 2010 Oct
PMID:Polymer-incarcerated metal(0) cluster catalysts. 2087 18

6,6-Dicyanopentafulvene (DCF) is a fascinating molecular entity that consists of a cyclopentadiene ring conjugated to an exocyclic double bond bearing two cyano groups on its periphery. Herein, we give a brief history of the chemistry of DCFs prior to our arrival to the field in 2011, followed by a summary of our work. We show how substitution on the ring and the exocyclic bond affects the HOMO and LUMO energies of pentafulvenes and how the design of DCFs was exploited computationally for the first time. Shortly after the report of the first rational synthesis of DCFs, we discovered that DCFs had a vast and astonishing array of reactivities to form new molecular entities. Simple, catalyst-free reactions between DCF acceptors and electron-rich donors led to the formation of scaffolds of exceptional complexity. Furthermore, our discovery that DCFs are capable of undergoing mild pentafulvene-to-benzene rearrangements challenges previous conventions of fulvene chemistry.
Chem Rec 2015 Feb
PMID:6,6-Dicyanopentafulvenes: teaching an old dog new tricks. 2530 96

We summarize the nonlinear optical (NLO) properties of octupolar molecules, crystals, and films developed in our laboratory. We present the design strategy, structure-property relationship, and second-order NLO properties of 1,3,5-trinitro- and 1,3,5-tricyano-2,4,6-tris(p-diethylaminostyryl)benzene (TTB) derivatives, TTB crystals, and films prepared by free-casting TTB in poly(methyl methacrylate) (PMMA). The first hyperpolarizability of TTB was fivefold larger than that of the dipolar analogue. Moreover, the TTB crystal showed unprecedentedly large second-harmonic generation (SHG). While TTB crystal films (20 wt% TTB/PMMA) on various substrates showed appreciable SHG values, the cylinder film exhibited much larger SHG values and large electro-optic (EO) coefficients. The large SHG values and EO coefficients, as well as the high thermal stability of the cylinder film, will make it a potential candidate for NLO device applications.
Chem Rec 2015 Feb
PMID:Octupolar molecules for nonlinear optics: from molecular design to crystals and films with large second-harmonic generation. 2531 98


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