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31.
Adachi K Sugiyama Y Yoneda K Yamada K Nozaki K Fuyuhiro A Kawata S 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(22):6616-6628
Novel triply hydrogen bonded suprastructures based on [M(tdpd)2(L)2]2- (H2tdpd=1,4,5,6-tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile, L=solvent) and melamine-analogous cations have been synthesized and characterized. The use of anions containing two AAA sets from [M(tdpd)2(L)2]2- together with cations containing one DDD set (A=hydrogen-bond acceptor, D=hydrogen-bond donor) leads to the formation of complementary triply hydrogen bonded modules in the solid state. In all cases, the building module is further extended via additional hydrogen-bonding interactions to produce a tape, and tapes are assembled into sheets. These results show that a hydrogen-bonded module consisting of different kinds of building blocks, one of which is a metal complex that includes hydrogen-bond acceptor sites and the other is a hydrogen-bond donor molecule, will be attractive for constructing metal-containing supramolecular systems by the self-assembly technique. 相似文献
32.
Sugiyama T Schweinberger E Kazimierczuk Z Ramzaeva N Rosemeyer H Seela F 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(2):369-378
2-Aza-2'-deoxyadenosine (2, z2Ad) is synthesized via its 1,N6-etheno derivative 7 and enzymatically deaminated to 2-aza-2'-deoxyinosine (3). Compound 2 is converted into the phosphoramidite building block 10b. This is employed in solid-phase oligonucleotide synthesis. The 2-azapurine base forms a strong base pair with guanine, but a much weaker one with adenine, thymine, and cytosine. Oligonucleotide duplexes with dangling nucleotide residues, such as 2-aza-2'-deoxyadenosine and 7-deaza-2'-deoxyadenosine (4, c7Ad), either on one or both termini, are synthesized, and the thermal stability of the duplexes is correlated with the hydrophobic properties of the dangling nucleotide residues. 相似文献
33.
The 7,8-bis(benzyloxy)bicyclo[2.2.2]octa-2,5-diene derivatives have been synthesized via Diels-Alder reaction of optically active 5,6-bis(benzyloxy)cyclohexa-1,3-diene and dienophiles. The corresponding tricarbonyliron complexes have also been synthesized in enantiomerically pure form. 相似文献
34.
Shoichi Katsuta Hirokazu Wakabayashi Mariko Tamaru Yoshihiro Kudo Yasuyuki Takeda 《Journal of solution chemistry》2007,36(4):531-547
Equilibria concerning picrates of tetraalkylammonium ions (Me4N+, Et4N+, Pr4N+, Bu4N+, Bu3MeN+) in a dichloromethane−water system have been investigated at 25 ∘C. The 1:1 ion-pair formation constants (K
IP,o
o) in dichloromethane at infinite dilution were conductometrically determined. The distribution constants (K
D
o) of the ion pairs and the free cations between the solvents were determined by a batch-extraction method. The K
IP,o
o value varies in the cation sequence, Bu4N+ ≈ Pr4N+ ≈ Et4N+ < Bu3MeN+ < < Me4N+; this trend is explained by the electrostatic cation−anion interaction taking into account the structures of the ion pairs
determined by density functional theory calculations. For the ion pairs of the symmetric R4N+ cations, there is a linear positive relationship between log10
K
D
o and the number of methylene groups in the cation (N
CH
2). The ion pair of asymmetric Bu3MeN+ has a higher distribution constant than that expected from the above log10
K
D
o
versus
N
CH
2 relationship. These cation dependencies of log10
K
D
o for the ion pairs are explained theoretically by using the Hildebrand-Scatchard equation. For all the cations, the log10
K
D
o value of the free cation increases linearly with N
CH
2; the variation of log10
K
D
o is discussed by decomposing the distribution constant into the Born-type electrostatic contribution and the non-Born one,
and attributed to the latter that is governed by the differences in the molar volumes of the cations. The cation dependencies
of the ion-pair extractability and ion pairing in water are also discussed.
An erratum to this article can be found at 相似文献
35.
36.
37.
A fully functionalized ABCD ring moiety of gambierol, a marine polycyclic ether toxin, was synthesized by the use of the oxiranyl anion strategy and reductive cycloetherification of a beta,delta-dihydroxy ketone. 相似文献
38.
Mariko Kitajima 《Tetrahedron letters》2006,47(19):3199-3202
A new pyrrolidinoindoline-type alkaloid, CPC-1, and a new tryptamine-derived dimeric alkaloid, CPC-2, were isolated from the seeds and rinds of Chimonanthus praecox f. concolor. The structure including the absolute configuration of CPC-1 was determined by chiral total synthesis. CPC-2 has a unique hexahydropyrroloquinoline skeleton. 相似文献
39.
An air-segmented continuous-flow method has been developed for the determination of molybdenum at ultra trace levels using
the catalytic effect of molybdate during the oxidation of L-ascorbic acid by hydrogen peroxide. Incorporation of an on-line
ion exchange column improved the tolerance limit for various ions. The detection limits with and without the column were 64 pmol L−1 and 17 pmol L−1, and the reproducibilities at 10 nmol L−1 were 2.1% and 0.2%, respectively. The proposed method was applied to the determination of molybdenum in seawater and lake
water as well as in rock and sediment samples. This method has the highest sensitivity among the available literature to our
knowledge, and is also convenient for routine analysis of molybdenum in various natural samples.
Author for correspondence. E-mail: masahito.sugiyama@ sojin0206.mbox.media.kyoto-u.ac.jp
Received October 23, 2002; accepted January 28, 2003
Published online May 19, 2003 相似文献
40.
A simple and highly sensitive method called thermal desorption (TD)-gas chromatography-mass spectrometry (GC-MS), which is used for the determination of trace amounts of 4-nonylphenol (NP) and 4-tert.-octylphenol (OP) in water samples, is described. NP and OP in samples are extracted from water samples and concentrated by the stir bar sorptive extraction (SBSE) technique. A stir bar coated with polydimethylsiloxane (PDMS) is added to a 2.0 ml water sample and stirring is carried out for 60 min at room temperature (25 °C) in a headspace vial. Then the extract is high sensitively analyzed by TD-GC-MS without any derivatization step. The optimum SBSE conditions are realized at an extraction time of 60 min. The detection limits are 0.02 ng ml−1 for NP and 0.002 ng ml−1 for OP. The method shows good linearity over the concentration range of 0.1-10 ng ml−1 for NP and 0.01-10 ng ml−1 for OP, and the correlation coefficients are higher than 0.999. The average recoveries of NP and OP are higher than 97% (R.S.D.: 3.6-6.2%) with correction using the added surrogate standards, 4-(1-methyl) octylphenol-d5 and deuterium 4-tert.-octylphenol. This simple, accurate, sensitive and selective analytical method may be used in the determination of trace amounts of NP and OP in tap and river water samples. 相似文献