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1.
Thawatchai Tuntulani Praput Thavornyutikarn Sirilux Poompradub Nongnuj Jaiboon Vithaya Ruangpornvisuti Narongsak Chaichit Zouhair Asfari Jacques Vicens 《Tetrahedron》2002,58(52):10277-10285
Tripodal aza crown ether calix[4]arenes, 5a, 5b, 6a and 6b, have been synthesized. The structure of protonated 5a was elucidated by X-ray crystallography to be a self-threaded rotaxane. Complexation studies of 5a and 5b towards anions using Na+ as countercation were carried out by 1H NMR titration in dimethylsulfoxide-d6 and the mixture of chloroform-d and methanol-d4, respectively. Ligands 5a and 5b were able to form 1:1 complexes with Br−, I− and NO3− and the complexation stability varied as follows: NO3−>I−>Br−. The effect of countercation on anion complexation was also investigated. The results showed that the association constants of 5a towards Br− in the presence of various cations varied as K+>Bu4N+>Na+. The enhancement in anion complexation ability of 5a may result from the rearrangement of the tripodal ammonium unit in the presence of K+. The neutral forms, 6a and 6b, were able to form complexes with transition metal ions such as Co2+, Ni2+, Cu2+ and Zn2+. The stability of the complexes followed the sequence: Ni2+2+Cu2+Zn2+. Compounds 6a and 6b may, therefore, potentially be used as either transition metal ion or anion receptors that can be controlled by pH of the solution. 相似文献
2.
Kessarin Ngamdee Theerapong Puangmali Thawatchai Tuntulani Wittaya Ngeontae 《Analytica chimica acta》2015
A new chemical sensor based on the measuring of circular dichroism signal (CD) was fabricated from cysteamine capped cadmium sulfide quantum dots (Cys-CdS QDs). The chiral-thiol molecules, d-penicillamine (DPA) and l-penicillamine (LPA), were used to evaluate potentials of this sensor. Basically, DPA and LPA provide very low CD signals. However, the CD signals of DPA and LPA can be enhanced in the presence of Cys-CdS QDs. The CD spectra of DPA and LPA exhibited a mirror image profile. Parameters affecting the determination of DPA and LPA were thoroughly investigated in details. Under the optimized condition, the CD signals of DPA and LPA displayed a linear relationship with the concentrations of both enantiomers, ranging from 1 to 35 μM. Detection limits of this sensor were 0.49 and 0.74 μM for DPA and LPA, respectively. To demonstrate a potential application of this sensor, the proposed sensor was used to determine DPA and LPA in real urine samples. It was confirmed that the proposed detection technique was reliable and could be utilized in a broad range of applications. 相似文献
3.
Anchalee Sirikulkajorn Thawatchai Tuntulani Boosayarat Tomapatanaget Anthony P. Davis 《Tetrahedron》2010,66(37):7423-520
A cholapod receptor possessing urea binding sites at C3, C7, and C12 positions and with an intrinsic chiral structure was synthesized, and the binding abilities toward amino acids in both l- and d- forms (Trp, Phe, Leu, and Ala) were studied using 1H NMR spectroscopy, UV-vis spectroscopy and computer simulation. Changes in 1H NMR spectra of the receptor revealed that complexation with amino acids occurred via hydrogen bonding and CH-π interactions. Binding to tryptophan was especially strong, and was found to be enantioselective (Ka=480 M−1 for l-Trp, 260 M−1 for d-Trp). NOESY and computer simulations were used to investigate the structures of the diastereomeric complexes between the receptor and the tryptophan enantiomers. In the case of l-Trp the carboxylate group bound at the two ureas adjacent to C7 and C12, while d-Trp was positioned closer to the urea adjacent to C3. 相似文献
4.
Rojrit Rojanathanes Thawatchai Tuntulani James B. Orton Michael B. Hursthouse Mongkol Sukwattanasinitt 《Tetrahedron》2005,61(5):1317-1324
Photo-switchable calixarenes consisting of a stilbene or azobenzene bridge, spanning the narrow rim as a switching unit, were synthesized through reductive coupling of o-, m- and p-bis-benzaldehyde and bis-nitrobenzene-substituted calix[4]arenes. Both cis- and trans-stilbenes were produced from the reductive coupling of the o- and m-bis-benzaldehyde with the cis isomer being predominant for both regioisomers, whilst the coupling of p-bis-benzaldehyde gave only cis product. On the other hand, the only isolable product obtained from the reductive coupling of bis-o- and bis-m-nitrobenzene was the corresponding trans-azobenzene and the coupling product from bis-p-nitrobenzene was not stable. Each of the synthesized compounds showed a photostationary state in their cis-trans isomerization. The complexation of alkali metal ions was observed for only the o-azobenzene derivative suggesting that the lone pair of N-atom in the azo bridge participates in this process. 相似文献
5.
A new circular dichroism sensor for detecting Ni2+ and Co2+ was proposed for the first time using chiral chelating quantum dots. The detection principle was based on changing of circular dichroism signals of the chiral quantum dots when forming a chiral complex with Ni2+ or Co2+. l-Cysteine capped cadmium sulfide quantum dots (l-Cyst-CdS QDs) were proposed as a chiral probe. The CD spectrum of l-Cyst-CdS QDs was significantly changed in the presence of Ni2+ and Co2+. On the other hand, other studied cations did not alter the original CD spectrum. Moreover, when increasing the concentration of Ni2+ or Co2+, the intensity of the CD spectrum linearly increased as a function of concentration and could be useful for the quantitative analysis. The proposed CD sensor showed linear working concentration ranges of 10–60 μM and 4–80 μM with low detection limits of 7.33 μМ and 1.13 μM for the detection of Ni2+ and Co2+, respectively. Parameters possibly affected the detection sensitivity such as solution pH and incubation time were studied and optimized. The proposed sensor was applied to detect Ni2+ and Co2+ in real water samples, and the results agreed well with the analysis using the standard ICP-OES. 相似文献
6.
Degradation of rhodamine B photocatalyzed by Eu-doped CdS nanowires illuminated by visible radiation
Anukorn Phuruangrat Siwat Thungprasert Thawatchai Sakhon Budsabong Kuntalue Titipun Thongtem Somchai Thongtem 《印度化学会志》2022,99(2):100349
CdS nanowires doped with different contents of Eu dopant were synthesized by solvothermal method. XRD, SEM, TEM and Raman analyses certified that the as-synthesized samples were hexagonal CdS uniform nanowires. The pure CdS nanowires were 1–3 ?μm long and 80 ?nm diameter with the 1st and 2nd order longitudinal phonon modes at 298 and 594 ?cm?1. The 3% Eu-doped CdS wires were 800 ?nm–2.5 ?μm long and 75 ?nm diameter with the 1st and 2nd order longitudinal phonon modes at 296 and 593 ?cm?1. CdS nanowires grew along the [001] direction due to the surface energy effect. The photocatalytic properties of CdS and Eu-doped CdS nanowires were investigated for the degradation of rhodamine B (RhB) illuminated by visible radiation. In this research, Eu dopant played the role in promoting the photocatalytic kinetics because Eu3+ ions act as an electron acceptor to promote charge separation and photocatalytic activity. Both ●OH and ●O2? were the main active radicals used to transform RhB molecules into CO2, H2O and other intermediates. 相似文献
7.
Chomchai Suksai Pannee Leeladee Colin Jennings Thawatchai Tuntulani Palangpon Kongsaeree 《Journal of chemical crystallography》2008,38(5):363-368
Abstract The reaction of 1,1′-bis(chlorocarbonyl)ferrocene with bis-aminobenzylcalix[4]arene gave amidoferrocene calix[4]arene monomer
1. Compound 1 crystallized in the monoclinic system P21/c with a = 11.196(6) ?, b = 14.971(11) ?, c = 32.007(2) ?, β = 96.413(4)° and V = 5330.9(6) ?3. X-ray diffraction analyses of 1 showed that the calix[4]arene scaffold was in cone conformation in which the intramolecular hydrogen bonding were formed
through OH groups at the lower rim to stabilize the structure. Moreover, the intramolecular hydrogen bond between the amide
groups of the amidoferrocene unit also presented in the crystal structure. On the other hand, the condensation of 1,1′-bis(chlorocarbonyl)ferrocene
with p-tert-bis-aminobenzylcalix[4]arene resulted in the monomeric 2 and [2 + 2] dimeric compounds 3. 1H-NMR studies signified that the calix[4]arene building block in compounds 2 and 3 adopted the cone conformation.
Index Abstract Synthesis and Characterization of Monomeric and Dimeric Structures of Calix[4]arenes Containing Amidoferrocene
Chomchai Suksai*, Pannee Leeladee, Colin Jennings, Thawatchai Tuntulani*, Palangpon Kongsaeree
The condensation of 1,1′-bis(chlorocarbonyl)ferrocene with p-tert-bis-aminobenzylcalix[4]arene resulted in the monomeric and [2 + 2] dimeric compounds.
相似文献
8.
Jansukra Piangkwan Wattanathana Worawat Duangthongyou Tanwawan Wannapaiboon Suttipong Songsasean Apisit Suramitr Songwut Tuntulani Thawatchai Browning C. Scott Wannalerse Boontana 《Journal of chemical crystallography》2021,51(4):523-535
Journal of Chemical Crystallography - 2-Chloro-N-(2,4-dinitrophenyl) acetamide, 1, was synthesized and characterized by 1H and 13C NMR spectroscopy, ESI–MS, X-ray crystallography, and... 相似文献
9.
A calix[4]arene-derived ditopic receptor 1 has been synthesized. In the absence of Na+, the receptor binds acetate in preference to diphenyl phosphate (as the tetrabutylammonium salts), but in the presence of Na+, the selectivity is reversed and the receptor, instead, binds diphenyl phosphate, and not acetate, which preferentially forms a salt ion-pair in free solution. [structure: see text] 相似文献
10.
Calix[4]arene derivatives containing amide ferrocene units at the wide rim and ethyl ester groups at the narrow rim, L1-L3, were synthesized and their anion binding and sensing properties were investigated. It was found from (1)H NMR titrations that L1-L3 were able to bind selectively with carboxylate anions. Moreover, cyclic voltammetry and square wave voltammetry showed that L1-L3 were able to act as electrochemical sensors for carboxylate anions. [structure: see text] 相似文献