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3.
Gong Y Xiang Y Yue B Xue G Bradshaw JS Lee HK Lee ML 《Journal of chromatography. A》2003,1002(1-2):63-70
Two bonded chiral stationary phases (CSPs), 8-aminoquinoline-2-ylmethyl- and 8-aminoquinoline-7-ylmethyl-diaza-18-crown-6-capped [3-(2-O-beta-cyclodextrin)-2-hydroxypropoxy]propylsilyl silica particles (non-porous, 1.5 microm), have been prepared and evaluated using capillary liquid chromatography at high pressures (> or = 8000 p.s.i.). High column efficiency (up to 400 000 plates m(-1)) was achieved for chiral separations. These CSPs with two recognition sites, i.e. substituted-diaza-18-crown-6 and beta-cyclodextrin combined with high chromatographic efficiency provide good resolution of a variety of enantiomers and positional isomers in relatively short times under reversed-phase conditions. After inclusion of a Ni (II) ion from the mobile phase, the positively charged crown ether-capped beta-cyclodextrin facilitates specific static, dipolar, and host-guest complexation interactions with solutes. 相似文献
4.
J. S. Bradshaw N. W. Adams R. S. Johnson B. J. Tarbet C. M. Schregenberger M. A. Pulsipher M. B. Andrus K. E. Markides M. L. Lee 《Journal of separation science》1985,8(10):678-683
Contemporary methods for the synthesis of alkyl- and arylsubstituted polysiloxane stationary phases are reviewed. A new, moderately polar phase containing the 3-(4-methoxyphenyl)-propyl group is reported. 相似文献
5.
Summary The chromatographic performance of newly developed dicyanobiphenyl polysiloxane stationary phases were evaluated and compared
with the performance of other polar stationary phases, including the previously reported monocyanobiphenyl polysiloxanes.
Due to the unique combination of polarizable biphenyl and polar cyano functionalities in the side chains of the flexible polysiloxane
backbone, and by virtue of their mild liquid crystalline properties, the new stationary phases provide excellent resolution
of a wide variety of analytes, both polar and nonpolar, in both GC and SFC. They can be easily coated and cross-linked in
open tubular columns, and the resultant columns demonstrate excellent efficiency and performance at temperatures up to 280–300°C.
The new stationary phases exhibit enhanced selectivities for various types of isomeric compounds. 相似文献
6.
J. Ty Redd Jerald S. Bradshaw Peter Huszthy Reed M. Izatt 《Journal of inclusion phenomena and macrocyclic chemistry》1997,29(3-4):301-308
Pyrimidino-crown ethers were prepared in 30-50% yields by reactingthe ditosylate derivative of the appropriate oligoethylene glycol with4-methoxy-5-methyl-2,6-pyrimidinedimethanol under basic conditions. A newmacrocyclic ligand containing a proton-ionizable pyrimidone subcyclic unitwas prepared in 88% yield by treating the appropriatepyrimidino-crown ether with 5 M NaOH in 50% (v/v) aqueous methanol.Preliminary complexation properties of some of these new compounds werestudied using various NMR spectral techniques. Good enantiomeric recognitionwas exhibited by a chiral pyrimidino-crown ether for the enantiomers of1-(-naphthyl)ethylammonium perchlorate. 相似文献
7.
Zhixian Zhou Hongna Han Tiesheng Li Yanjun Xing Yangjie Wu Xian Xin Zhang Reed M. Izatt N. Kent Dalley Jerald S. Bradshaw Weijie Chai Cunheng He 《Structural chemistry》1999,10(3):177-185
Reactions of CsI and HgI2 with benzo-15-crown-5 (B15C5) and 15-crown-5 (15C5) in an ethanol-acetone mixture produced [Cs(B15C5)2]2[Hg2I6] (1) and {[Cs(15C5)]2[Hg2I6]}n (2), respectively. The structures of the two complexes are quite different. Molar ratios of Cs+ : crown ether are 1 : 2 in 1 and 1 : 1 in 2. Complex 1 consists of two Cs(B15C5)
2
+
cations and a Hg2I
6
2-
anion. Cs+ lies between the two crown-5 ligands, resulting in a sandwich-type cation. Cationic Cs(B15C5)
2
+
and anionic Hg2I
6
2-
are linked together by electrostatic interactions and the complex 1 is an ion pair compound. Complex 2 consists of infinite [Cs(15C5)]2[Hg2I6] units. Each structural unit contains two Cs(15C5)+ cations and a Hg2I
6
2-
anion. Cs+ is coordinated by five oxygen atoms of 15C5, three iodine atoms of Hg2I
6
2-
, and an iodine atom of Hg2I
6
2-
in an adjacent structural unit. The interactions between the Cs+ of Cs(15C5)+ and an I– in Hg2I
6
2-
from adjacent structural units polymerize the complex 2, resulting in a one-dimensional network structure. The anions of Hg2I
6
2-
in both complexes are similar. The two mercury atoms are linked through two bridging iodine atoms and each mercury is also coordinated by two terminal iodines. Crystal data for 1: space group P21/c (No. 14), a = 12.253(4), b = 20.945(7), c = 16.110(6) Å, = 111.0(1)°, V = 3860 Å3, Z = 4, R = 0.082 (R
w = 0.089). Crystal data for 2: space group P21/c (No. 14), a = 12.157(4), b = 8.546(4), c = 20.666(6) Å, = 91.54(3)°, V = 2146 Å3, Z = 4, R = 0.034 (R
w = 0.048). 相似文献
8.
Jerald S. Bradshaw Reed M. Izatt James J. Christensen Krzystof E. Krakowiak Bryon J. Tarbet Ronald L. Bruening S. Lifson 《Journal of inclusion phenomena and macrocyclic chemistry》1989,7(2):127-136
Silica gel-bound crown ethers and aza macrocycles have been synthesized with the attaching arm connected to the carbon framework of the macrocycles. The interactions of these bound macrocycles with cations are almost identical to those involving the analogous free macrocycles. This has allowed for predictable cation separation, concentration, and removal processes to be performed on a small scale. Quantum mechanical calculations and NMR measurements indicate that similarly bound chiral macrocycles will be capable of use in separating chiral organic amines.Dedicated to the memory of Professor James J. Christensen who died on 5 September 1987. 相似文献
9.
Reed M. Izatt Gypzy C. Lindh Peter Huszthy Glen A. Clark R. L. Bruening Jerald S. Bradshaw James J. Christensen 《Journal of inclusion phenomena and macrocyclic chemistry》1989,7(5):501-509
The macrocycle-mediated fluxes of alkali, alkaline earth, and several transition metal cations have been determined and compared in a H2O-CH2Cl2-H2O liquid membrane system using four water-insoluble macrocycles containing a dialkylhydrogenphosphate moiety. Transport of alkali metal cations by these ligands was greatest from a source phase pH = 12 or above into an acid receiving phase (pH = 1.5). Very low fluxes were observed for the transport of the alkaline earth cations and all transition metal ions studied except Ag+ and Pb2+ which were transported reasonably well by these new macrocycles.Deceased: September 5, 1987. 相似文献
10.
Tingmin Wang Jerald S. Bradshaw Janet C. Curtis Peter Huszthy Reed M. Izatt 《Journal of inclusion phenomena and macrocyclic chemistry》1993,16(2):113-122
Significant - interaction is found in the complexes of (S, S)-dimethylpyridino-18-crown-6 with (R)- and (S)-[-(1-naphthyl)ethyl]ammonium perchlorate. This finding is supported by the1H NOESY NMR spectral technique, greater chemical shift changes of aromatic protons in both host and guest molecules upon complexation, and by molecular mechanics calculations. Because of the flexibility of the ligand, the tripod hydrogen bonding causes13C relaxation times of all periphery carbons to decrease without significant selectivity. Rotational energy barrier calculations of the methyl groups of the complexed ligand also show that the (S, S)-host-(R)-guest is the more stable complex. 相似文献