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Xiao-Ming Chen

Publications and source records attributed to Xiao-Ming Chen.

At least 19 recordsLinked to original sources
PubMed2006

Two mixed-valence vanadium(III,IV) phosphonoacetates with 16-ring channels: H2(DABCO)[V(IV)O(H2O)V(III)(OH)(O3PCH2CO2)2].2.5H2O and H2(PIP)[V(IVO)(H2O)V(III)(OH)(O3PCH2CO2)2].2.5H2O.

Two isostructural mixed-valence vanadium phosphonoacetates H2(DABCO)[V(IV)O(H2O)V(III)(OH)(O3PCH2CO2)2].2.5H2O (1) and H2(PIP)[V(IV)O(H2O)V(III)(OH)(O3PCH2CO2)2].2.5H2O (2) have been synthesized. They crystallize in the orthorhombic space group Pnna with a = 7.0479(10) A, b = 15.307(2) A, and c = 17.537(3) A for 1 and a = 7.0465(9) A, b = 15.646(2) A, and c = 17.396(2) A for 2. X-ray single-crystal diffraction reveals that 1 and 2 have a three-dimensional open framework featuring 16-ring ellipsoid channels that are filled with doubly protonated 1,4-diazabicyclo[2,2,2]octanium/piperazinium cations and water molecules. According to the classification in metal-organic frameworks, 1 and 2 contain infinite (-O-V-)(infinity) chains that are cross-linked by "metalloligand" [VO(H2O)(O3PCH2CO2)2](4-) into a 3-D net of the sra topology. The temperature dependence of the magnetic susceptibility of 1 shows that the chi(m)T value in the range of 60-320 K is constant of 1.105 cm3 K mol(-1)/V2 unit, and upon further cooling, the chi(m)T value rapidly increases to 1.81 cm3 K mol(-1) at 2 K. The corresponding effective magnetic moment (mu(eff))/V2 unit varies from 2.97 mu(B) at 320 K to 3.80 mu(B) at 2 K. The magnetic data in the range of 2-320 K follow the Curie-Weiss law with C = 1.074 cm3 K mol(-1) and Theta= -1.34 K.

Journal Article↗
PubMed2006

Chiral magnetic metal-organic frameworks of dimetal subunits: magnetism tuning by mixed-metal compositions of the solid solutions.

The isostructural, chiral molecular magnetic materials with the formula [MxM'(2-x)(ca)2(1,4-dimb)]n [H2ca = D-(+)-camphoric acid, 1,4-dimb = 1,4-di-(1-imidazolyl-methyl)-benzene, M = Ni(II), M' = CoII, 0 < or = x < or = 2] consist of ca-bridged (4,4) layers with [M2(O2CR)4] as secondary building units that are pillared by the 1,4-dimb ligands into a unique 3D framework. The high-spin octahedral symmetry and the proportions of the mixed-metal ions were characterized by UV-vis spectroscopy. The compounds exhibit the onset of antiferromagnetic ordering at 7.5 approximately 23 K, as well as weak ferromagnetism, spin-flop, and glassy behavior that result from the randomness of the mixed-metal pairs, magnetic anisotropy of the metallic cations, and antisymmetric exchange. The composites should be regarded as molecular alloys of the pure Ni(II) and Co(II) compounds. The magnetic behavior of the solid solutions shows unambiguously that the organic bridges, bond angles, and bond distances greatly influence the effective interactions and bring about cooperative magnetic behavior in the chiral 3D frameworks.

Cobalt↗
PubMed2006

A robust microporous 3D cobalt(II) coordination polymer with new magnetically frustrated 2D lattices: single-crystal transformation and guest modulation of cooperative magnetic properties.

A microporous 3D cobalt(II) coordination polymer featuring pillared layers [Co(2)(ma)(ina)](n) x 2nH(2)O (1 x 2H(2)O) (ma = malate, ina = isonicotinate) was generated by hydrothermal treatment with a void volume of 25.8%, in which the in-situ generated ma ligands connect the Co(II) ions into a 2D lattice with mixed and multiple exchange-bridges, affording a new geometrical topology different from the Kagomé lattice and leading to spin frustration. The rigid ina-pillared metallic-layered structure could retain 3D structural ordering upon guest removal and exchange. By soaking guest-free host in MeOH and methanamide (HCONH(2)) solutions, single crystals of dehydrated were transformed into single crystals of 1 x MeOH and 1 x HCONH(2), respectively, without apparent host-structural changes. 1 can also be rehydrated into 1 x 2H(2)O'. The guest-inclusion crystals have been characterized by X-ray single-crystal diffraction at 293 K and 93 K, confirming the single-crystal-to-single-crystal transformations and providing detailed information of the guest molecules confined in the subnanospace and host-guest and/or guest-guest hydrogen-bonding interactions. The magnetic behaviours of this family of porous magnetic materials are complex due to the influences of multiple metal sites, intra- and inter-layer exchanges, spin-orbit coupling, as well as geometrical frustration, which show magnetic ordering at <2 K, 3.5 K, 3.5 K, and 8 K for 1, 1 x MeOH, 1 x HCONH(2), and 1 x 2H(2)O, respectively, due to the different size of guest molecules along with the different host-guest interaction, which may slightly modify the path of magnetic exchange, decrease the intensity of the spin-frustration in the 2D lattice, and cooperatively enhance the magnetic ordering temperature.

Journal Article↗
PubMed2006

Crystal engineering of binary metal imidazolate and triazolate frameworks.

This article summarizes the recent advances in the crystal growth, structural control strategies and diverse structures of the binary metal imidazolate and triazolate frameworks, which are the simplest systems for crystal engineering of two-, three- and four-connected coordination polymers.

Journal Article↗
PubMed2006

One-pot synthesis of polysaccharide 3,5-dimethylphenylcarbamates having a random vinyl group for immobilization on silica gel as chiral stationary phases.

Different kinds of vinyl groups were randomly introduced onto the glucose units of cellulose 3,5-dimethylphenylcarbamates by a one-pot method using the bifunctional reagents dec-1-ene-10-isocyanate, 2-isocyanatoethyl methacrylate, and methacryloyl chloride. The chiral recognition properties of the prepared derivatives were then evaluated by coating and immobilizing them on silica gel as HPLC packing material. Immobilization was carried out by radical copolymerization with a vinyl comonomer, 1,5-hexadiene, in toluene at 80 degrees C. The effects of the structures and content of the vinyl groups on the immobilization and on enantioseparations were investigated. This one-pot method was also extended to the synthesis of amylose 3,5-dimethylphenylcarbamates having a random vinyl group. Comparisons of the chiral resolution powers of our laboratory-made packing materials and the newly commercialized Chiralpak IA with immobilized amylose 3,5-dimethylphenylcarbamate and Chiralpak IB with immobilized cellulose 3,5-dimethylphenylcarbamate are discussed.

Amylose↗
PubMed2006

Association of cytomegalovirus infection with human leukocyte antigen genotypes in recipients after allogeneic liver transplantation.

BACKGROUND: Cytomegalovirus (CMV) infection is the important cause affecting the survival rate and function of the transplanted organ after transplantation. The occurrence of CMV infection after liver transplantation (LT) is associated with many factors. Lots of studies suggest that genetic mutation between hosts and CMV may play a role in the occurrence and development of CMV infection. CMV exists in an incubative state, affect or destroy the expression of human leukocyte antigen (HLA) molecules in the host cell surface, and interfere antigen's submission. This mechanism is the key of CMV to avoid immune defense mechanism of the host. To detect HLA and CMV antibody (CMV-Ab), CMV antigen (CMV-Ag) of transplantation recipients, we evaluated the association of CMV infection and the particular HLA genotypes in recipients after LT. METHODS: 277 blood samples were collected from 39 LT recipients. CMV antibody and antigen were detected by ELISA or immunohistochemical methods. The HLA types of the recipients were determined by PCR. To analyze the association of HLA alleles and the occurrence of CMV antigenemia in the patients, relative risk degree (RR) was used as the parameter for the Chi-square test. RESULTS: The LT recipients were serum CMV IgG positive (100%), but none of them was CMV IgM positive (0%). Thirty-three LT recipients (84.6%) were CMV antigenic positive with 1-50 positive leukocytes per 50,000 leukocytes in extent and 7.2+/-4.2 positive leukocytes per 50,000 leukocytes on average. Thirteen patients developed CMV pneumonia, with CMV antigenic positive (100%) and 17.7+/-5.5 positive leukocytes per 50,000 leukocytes on average. Some HLA alleles were associated with the occurrence and extent of CMV antigenemia. HLA-A2 was the higher frequency allele for patients with antigenemia (P<0.05), and 7 patients carrying HLA-DR11 allele developed antigenemia (P<0.05). In the lower antigenemia group, HLA-A11 was higher in frequency than others (P<0.05). Besides, none of the patients carrying HLA-B16 allele developed clinical symptoms of CMV infection (P<0.05). CONCLUSIONS: The variability of HLA alleles might modulate immune response to CMV infection. HLA examination before transplantation should be made for prevention and treatment of CMV infection after operation.

Adolescent↗
PubMed2005

Influence of vinyl monomers and temperature on immobilization of cellulose 3,5-dimethylphenylcarbamate onto silica gel as chiral stationary phases for high-performance liquid chromatography.

Cellulose 3,5-dimethylphenylcarbamates bearing a low content of a vinyl group at the 6-position on the glucose units were synthesized by a previously developed regioselective method and chemically immobilized onto a vinylized silica gel as chiral stationary phases (CSPs) for high-performance liquid chromatography (HPLC). The immobilization of the derivatives was performed through a radical polymerization reaction with AIBN as the initiator in the presence of toluene. The effects of vinyl monomers, such as isoprene, 2,3-dimethyl-1,3-butadiene (DMBD), ethylene glycol dimethacrylate (EDMA) and 1,5-hexadiene, on the immobilization and enantioselectivities of the derivatives were investigated. The effect of the temperature used for the radical polymerization reaction on the immobilization was also examined. In addition, the direct comparison of the chiral recognition abilities of the laboratory-made and commercially available columns was discussed.

Carbamates↗
PubMed2005

Determination of platelet-activating factor by reverse phase high-performance liquid chromatography and its application in viral hepatitis.

AIM: To detect the platelet-activating factor (PAF) and the plasma or serum levels of tumor necrosis factor-alpha (TNF-alpha) malondialdehyde (MDA), endotoxin (ET) and to discuss their significance in various types of viral hepatitis. METHODS: PAF, TNF-alpha, MDA, and ET levels in 60 controls, 16 cases of acute viral hepatitis, 71 cases of chronic viral hepatitis, 19 cases of severe viral hepatitis were detected by reverse phase high-performance liquid chromatography (rHPLC), bio-assay, ELISA, thiobarbituric acid (TBA), and limulus lysate test (LLT), respectively. RESULTS: The rHPLC was more sensitive and specific than bio-assay (r = 0.912, P<0.01). The plasma levels of PAF, TNF-alpha, MDA, and ET in patients with viral hepatitis were higher than those in controls (P<0.01). CONCLUSION: rHPLC is more reliable and accurate for the detection of PAF.

Adult↗
PubMed2005

Pillared-layer microporous metal-organic frameworks constructed by robust hydrogen bonds. Synthesis, characterization, and magnetic and adsorption properties of 2,2'-biimidazole and carboxylate complexes.

Two new isostructural complexes [M(H2biim)3][M(btc)(Hbiim)].2H2O (M = Co, (1); M = Ni, (2)) (btc = 1,3,5-benzenetricarboxylate; H2biim = 2,2'-biimidazole) have been synthesized and characterized by single-crystal X-ray diffraction. They present a unique structure consisting of two distinct units: the monomeric cations [M(H2biim)3]2+ and the two-dimensional (2D) anionic polymer [M(Hbiim)(btc)]2-. In the anionic moiety, the Hbiim- monoanion is simultaneously coordinated to one metal atom in a bidentate mode and further to another metal atom in a monodentate mode. The imidazolate groups bridge the two adjacent metal ions into a helical chain which is further arranged in left- and right-handed manners. These chains are bridged by btc ligands into a 2D brick wall structure. The most interesting aspect is that the [M(H2biim)3]2+ cations act as pillars and link the anionic layers via robust heteromeric hydrogen-bonded synthons (9) and (7) formed by the uncoordinated oxygen atoms of carboxylate groups and the H2biim ligands, resulting in a microporous metal-organic framework with one-dimensional (1D) channels (ca. 11.85 angstroms x 11.85 angstroms for 1 and 11.43 angstroms x 11.43 angstroms for 2). Magnetic properties of these two complexes have also been studied in the temperature range of 2-300 K, and their magnetic susceptibilities obey the Curie-Weiss law in the temperature range of 20-300 K (for 1) and 2-300 K (for 2), respectively, showing anti-ferromagnetic coupling through imidazolate bridging. Taking into consideration the Heisenberg infinite chain model as well as the possibility of chain-to-chain and chain-to-cation interactions, the anti-ferromagnetic exchange of 2 is analyzed via a correction for the molecular field, giving the values of g(cat) = 2.296, g(Ni) = 2.564, J = -13.30 cm(-1), and zJ' = -0.017 cm(-1). The microporous frameworks are stable at ca. 350 degrees C. They do not collapse after removal of the guest water molecules in the channels, and they adsorb methanol molecules selectively.

Journal Article↗
PubMed2005

Synthesis, structures, and magnetic properties of heteronuclear Cu(II)-Ln(III) (Ln = La, Gd, or Tb) complexes.

Facile one-pot reactions led to the formations of dinuclear [CuLn(hmp)2(NO3)3(H2O)2] (Ln = Tb (1.Tb), Gd (1.Gd), or La (1.La)), and trinuclear [Cu2Ln(mmi)4(NO3)(H2O)2](ClO4)(NO3).2H2O (Ln = Tb (2.Tb) or Gd (2.Gd)) and [Cu2La(mmi)4(NO3)2(H2O)](ClO4).2H2O (2.La) with polydentate ligands 2-(hydroxymethyl)-pyridine and 2-hydroxymethyl-1-methyl-imidazole. In these complexes, each pair of Cu(II) and Ln(III) ions is linked by a double mu-alkoxo bridge. The temperature dependences of the magnetic susceptibilities of 1 and 2 were investigated in the range of 2-300 K. The dinuclear and trinuclear Cu-Gd complexes exhibit ferromagnetic interaction. The coupling constant J values in the heterodinuclear Cu-Gd complexes are correlated to values of the dihedral angles alpha between the two O-Cu-O and O-Gd-O fragments of the bridging CuO2Gd networks, with the largest J value associated with the smallest alpha value. The occurrence of a ferromagnetic interaction between Cu(II) and Gd(III) ions of the trinuclear entity is supported by the field dependence of the magnetization. The field dependence of the magnetization at 2 K of 1.Gd and 2.Gd confirms the nature of the ground state and of the Cu(II)-Gd(III) interaction, while alternating current susceptibility measurements demonstrates out-of-phase ac susceptibility signals of 1.Tb, which is the molecule-based magnetic material of the smallest nuclearity which exhibits frequency-dependent behavior within the 3d-4f mixed-metal systems.

Journal Article↗
PubMed2005

Temperature- or guest-induced drastic single-crystal-to-single-crystal transformations of a nanoporous coordination polymer.

Aside from a temperature-induced structural transformation, a new nanoporous coordination polymer [Ag6Cl(atz)4].OH.6H2O (Hatz = 3-amino-1,2,4,-triazole) comprised of interpenetrated Ag3(atz)2 coordination nets exhibits a single-crystal-to-single-crystal transformation of a 5-fold to 6-fold net interpenetration change triggered by guest desorption/absorption.

Crystallization↗
PubMed2005

Supramolecular isomerism within three-dimensional 3-connected nets: unusual synthesis and characterization of trimorphic copper(I) 3,5-dimethyl-1,2,4-triazolate.

Solvothermal treatments of acetonitrile, aqueous ammonia and copper(II) salts frequently yielded alpha-[Cu(mtz)](1)(Hmtz = 3,5-dimethyl-1,2,4-triazole) under different reaction conditions. However, two new supramolecular isomers of 1, namely beta-[Cu(mtz)](2) and gamma-[Cu(mtz)](3) were successfully isolated upon introducing 4,4'-bipyridine or nitrate as an additive. 1-3 represent the first example of true supramolecular isomerism within 3D 3-connected nets. Besides the 4.8.10 net for the tetragonal phase 1 (P4(2)/n, a= 13.470(2), c= 6.142(2)A), two novel 3-connected nets, 8(2)10-a and 6.10(2), were observed in the new tetragonal phase 2 (I42d, a= 14.0247(5), c= 5.2884(4)A) and orthorhombic phase 3 (Iba2, a= 8.0423(7), b= 11.5310(10), c= 17.3505(16)A), respectively. The three isomers also displayed distinct physical properties related to their different supramolecular structures.

Journal Article↗
PubMed2005

Hydrogen-bonded anionic rosette networks assembled with guanidinium and C3-symmetric oxoanion building blocks.

Two premeditated anionic rosette-layer architectures have been constructed using guanidinium and ubiquitous C3-symmetric oxoanions that carry unequal charges, employing bulky organic cations as interlayer templates. The undulate guanidinium-carbonate network occurs in 4[(C2H5)4N+].8[C(NH2)3+].3(CO3)2-.3(C2O4)2-.2H2O, in which the disordered (C2H5)4N+ guests are accommodated in pouches and channels within a complex three-dimensional hydrogen-bonded host framework. In [(C2H5)4N+]2.[C(NH2)3+].[1,3,5-C3H3(COO-)3].6H2O, ordered (C2H5)4N+ cations are sandwiched between planar guanidinium-trimesate host layers whose honeycomb cavities are tightly fitted with flattened-chair (H2O)6 clusters of symmetry 2.

Anions↗
PubMed2005

Syntheses, structures, photoluminescence, and theoretical studies of a class of beryllium(II) compounds of aromatic N,O-chelate ligands.

Three members of a new class of luminescent, neutral, and monomeric Be(II) complexes of aromatic N,O-chelate ligands, namely [Be(pbm)(2)] (1), [Be(pbx)(2)] (2), and [Be(pbt)(2)] (3) [Hpbm = 2-(2'-hydroxylphenyl)benzimidazole, Hpbx = 2-(2'-hydroxylphenyl)benzoxazole, and Hpbt = 2-(2'-hydroxylphenyl)benzothiazole], have been prepared and characterized by X-ray crystallography and photoluminescence studies. All the complexes are neutral, mononuclear molecules and display strong photoluminescence in the blue/green region, and thus, they may serve as candidates for electroluminescence materials. The electronic transitions in the photoluminescent process have also been investigated by means of time-dependent density functional theory (TDDFT) energy level and molecular-orbital analyses, showing that their absorption and luminescent properties are ligand-based and ligand-tunable.

Journal Article↗