New highly stereoregular 2, 3 -di- O-(p-azidobenzyl )-(1 →5 ) - α-D -ribofuranan was synthesized byselective ring-opening polymerization of 1, 4-anhydro-2, 3 - di-O -(p-azidobenzyl )-α-D -ribopyranose(ADABR) using ...New highly stereoregular 2, 3 -di- O-(p-azidobenzyl )-(1 →5 ) - α-D -ribofuranan was synthesized byselective ring-opening polymerization of 1, 4-anhydro-2, 3 - di-O -(p-azidobenzyl )-α-D -ribopyranose(ADABR) using phosphorus pentafluoride or tin tetrachloride as catalyst at low temperature indichloromethane. The monomer was obtained by the reaction of p - bromomethyl -phenyleneazide with 1, 4 -anhydro-α-D-ribose in DMF. The structure of poly(ADANR) was identified by specific rotation and ^(13)C-NMR spectroscopy. Acid chloride-AgCl_4 complex catalyst such as CH_2=C(CH_3)C^+OClO_4^- used in thepolymerization resulted in polymers with mixed structures, i.e. (1→5)-α-D-ribofuranosidic and (1→4)-β-D-ribopyranosidic units. However, with C_6H_5C^+OClO_4^- as catalyst, pure (1→5)-α-D-ribofuranan was obtained.The effects of catalyst, polymerization temperature and time on polymer stereoregularity were examined, andthe mechanism of the ring-opening polymerization was discussed.展开更多
The complex [Ni(L)(N3)2](H_2O (L=N,N(-Bis(2-pyridylaldehyde) condensation 1,3-diaminopropane) was synthesized by the reaction of NiCl2(6H_2O with 2-pyridylaldehyde and 1,3-diaminopropane and sodium azide in the ethan...The complex [Ni(L)(N3)2](H_2O (L=N,N(-Bis(2-pyridylaldehyde) condensation 1,3-diaminopropane) was synthesized by the reaction of NiCl2(6H_2O with 2-pyridylaldehyde and 1,3-diaminopropane and sodium azide in the ethanol. A single-crystal X-ray study shows that the complex is a six-coordinated nickel (II) with an octahedral environment compound (C15H18N10NiO). The crystal is orthogonal, space group Pbca, with unit cell parameters: a = 13.577(3), b = 15.261(3), c = 17.554(4) ?, V= 3637(1) ?3, Z=8, Mr=413.10, Dc=1.509 g/cm3, ( = 1.096 mm－1, F(000) = 1712, T = 293(2)K, R = 0.0411, wR = 0.1048 for 2888 reflections with I >2( (I). The distances between Ni and N atoms (N(1), N(2), N(3), N(4)) range from 2.050(2) to 2.140(2)?. The distances of Ni-N(5) and Ni-N(8) are 2.115(3) and 2.133(3)?, respectively. The solvent molecule H_2O(O(1)) is linked by hydrogen bonds with O(1) and N(5) and N(8) atoms. Their distances are 2.881(+x, +y, +z) and 2.893(0.5+x, y, 0.5+z)?, respectively.展开更多
A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts ...A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts of stable, non-radioactive labeled DNA and RNA hybridization probes. And it is supposed to be easily detected for its photochromic properties.展开更多
A new thiolate-bridged diiron complex with two mono-coordinated azido ligands, [Cp＊Fe（kt-SMe）N3]2 （Cp^＊ = η^5-C5Me5）, was synthesized from [Cp＊Fe（η-SMe）MeCNMPF6]2 and NaN3 in a bi-solvent system of acetone ...A new thiolate-bridged diiron complex with two mono-coordinated azido ligands, [Cp＊Fe（kt-SMe）N3]2 （Cp^＊ = η^5-C5Me5）, was synthesized from [Cp＊Fe（η-SMe）MeCNMPF6]2 and NaN3 in a bi-solvent system of acetone and methanol. X-ray crystal structural analysis shows that the compound belongs to the orthorhombic Fdd2 space group, with a = 14.3771（15）, b = 71.424（8）, c = 9.7010（10）A, V = 9961.7（18） A3, C22H36Fe2N6S2, Mr = 560.39, Dc = 1.495 g/cm^3, F（000） = 4704,μ（MoKa） = 1.355 mm-I and Z = 16. The compound consists ofa di（u-thiolate）diiron unit {Cp＊Fe（p-SMe）}2, in which each iron is coordinated by a terminal azido ligand. Magnetic characterizations show spin canting behavior for the title compound.展开更多
The organic-inorganic hybrid complex with formula [（CuL）2Cu3（μ-1,1-N3）4（ClO4）2], complex 1, {CuL, [5,6：14,l5-dibenzo-1,4,8,12-tetraazacyclopentadeca-7,3-diene-2,3-dione（2-）]copper（Ⅱ）}, has been synthesize...The organic-inorganic hybrid complex with formula [（CuL）2Cu3（μ-1,1-N3）4（ClO4）2], complex 1, {CuL, [5,6：14,l5-dibenzo-1,4,8,12-tetraazacyclopentadeca-7,3-diene-2,3-dione（2-）]copper（Ⅱ）}, has been synthesized and structurally determined. The crystals of complex 1 crystallize in the triclinic system with space group P1, a=0.92983（12） nm, b=1.09644（14） nm, c=1.27396（16） nm, α=70.782（2）°β=86.266（2）°,γ=78.284（2）°. In this complex, the five copper ions are bridged by macrocyclic oxamide groups and azido. Furthermore, C-H…O hydrogen bond interactions link the pentanuclear fragments to form a 2D supramolecular architecture.展开更多
Poly[styrene(iodosodiacetate)] reacted with diaryl diselenides, followed by sodium azide, giving 1-azido-2-arylselenoalkanes regioselectively. The polymer reagent could be regenerated and reused.
The 1-azido-2-chloro-4-nitrobenzene was prepared by nucleophilic substitution between 2-chloro-4-nitro-1-(trifluoromethylsulfinyl)benzene and sodium azide, and its structure was characterized by NMR spectrum and X-ray...The 1-azido-2-chloro-4-nitrobenzene was prepared by nucleophilic substitution between 2-chloro-4-nitro-1-(trifluoromethylsulfinyl)benzene and sodium azide, and its structure was characterized by NMR spectrum and X-ray single-crystal diffraction. It crystallizes in the monoclinic system, space group P21/n, Z = 8 and Mr = 198.57. A cultivation process of the single crystal of unstable aryl azide was provided. The group of trifluoromethyl sulfinyl was found for the first time to be a new excellent leaving group of aromatic nucleophilic substitution reactions.展开更多
A novel one-dimensional manganese(II) complex containing nitronyl nitroxide radical [Mn2(IM2-py)2(Ac)2(μ1,1-N3)(μ1,3-N3)·EtOH]n was synthesized and characterized structurally and magnetically. It crystallizes i...A novel one-dimensional manganese(II) complex containing nitronyl nitroxide radical [Mn2(IM2-py)2(Ac)2(μ1,1-N3)(μ1,3-N3)·EtOH]n was synthesized and characterized structurally and magnetically. It crystallizes in the monoclinic space group p21/n. Each Mn(II) ion is six-coordinated in a distorted octahedral environment. The two N atoms of the nitronyl nitroxide radical and the two O atoms of acetate ligands are in the equatorial plane, whereas the two different azido bridging ligands are in trans axial position. Mn(II) ions are linked by nitrogen atom of μ1,1-azido and oxygen atoms of two carboxy groups to form a Mn-Mn unit. Mn-Mn units are linked by azido ligands through μ1,3 bridging style to form a one-dimensional chain. The compound is connected by the coordination bonds, π-π interactions and hydrogen bonds as a three-dimensional structure. Magnetic susceptibility data support that there are stronger antiferromagnetic interactions between the radical and Mn(II) ion, weak antiferromagnetic interactions between the Mn-R units, and very weak antiferromagnetic interactions between the R-Mn-Mn-R units.展开更多
A coordination polymer formulated as {[Mn2L（N3）4]·2H2O）n（1） [L = 1,4-bis（pyridinil-3-carboxylato）-1,4- dimethylbenzene] was synthesized and structurally and magnetically characterized. The uniform Mn（Ⅱ）...A coordination polymer formulated as {[Mn2L（N3）4]·2H2O）n（1） [L = 1,4-bis（pyridinil-3-carboxylato）-1,4- dimethylbenzene] was synthesized and structurally and magnetically characterized. The uniform Mn（Ⅱ） chains with mixed （μ-EO-N3）2（μ-COO） triple bridges （EO = end-on） are linked by L ligands to generate a 2-fold interpenetrating 3D framework. Meanwhile, magnetism analysis reveals antiferromagnetic coupling for 1.展开更多
2-Azido-4-nitroimidazole and its derivatives have been synthesized for energetic material applications. The synthesized compounds were fully characterized by 1H, 13C NMR spectroscopy and elemental analysis. Most of th...2-Azido-4-nitroimidazole and its derivatives have been synthesized for energetic material applications. The synthesized compounds were fully characterized by 1H, 13C NMR spectroscopy and elemental analysis. Most of them were determined by single crystal X-ray diffraction. The calculated densities of the compounds range between 1.71 and 1.92 g,cm-3. The calculated detonation pressures （P） for these derivatives fall in the range of 25.17 to 32.62 GPa and the detonation velocities （D） are distributed from 7.65 to 8.55 km·s-1.展开更多
The 2-azido-4-nitroimidazole-based energetic salts were synthesized in a simple and straightforward manner. The structures of these new salts were determined by IR, 1H NMR and 13C NMR spectroscopy and elemental analys...The 2-azido-4-nitroimidazole-based energetic salts were synthesized in a simple and straightforward manner. The structures of these new salts were determined by IR, 1H NMR and 13C NMR spectroscopy and elemental analysis. These salts also exhibited high positive enthalpies of formation, high nitrogen content, and moderate detonation properties.展开更多
The development of azide migration reactions is a formidable challenge due to potential competition from side processes driven by the release of molecular nitrogen. Here, we show a novel neighbouring carbonyl group-as...The development of azide migration reactions is a formidable challenge due to potential competition from side processes driven by the release of molecular nitrogen. Here, we show a novel neighbouring carbonyl group-assisted sequential 1,2-azide and 1,4-oxygen migration reaction of α-vinyl azides for the efficient preparation of a range of α-azido ketones. This represents the first transformation of α-vinyl azides into α-azido ketones. Notable features of this method are its high efficiency, broad substrate scope, excellent functional group compatibility, and high yields. The computational studies gave a key insights into the regioselective 1,2-azide and 1,4-oxygen migrations assisted by the neighbouring carbonyl group. Further conversions into a variety of nitrogen-containing compounds demonstrated the synthetic utility of the α-azido ketone products. Preliminary mechanistic studies disclosed a novel reaction mechanism involving neighbouring carbonyl group-assisted sequential 1,2-azide and1,4-oxygen migrations.展开更多
The geometries, heats of formation and electronic structures of 15 azido-derivatives of 1,2,3-TNB (I), 1,2,4-TNB (II) and 1,3,5-TNB (III) have been studied using quantum chemical AM1 method at HF level. The effect of ...The geometries, heats of formation and electronic structures of 15 azido-derivatives of 1,2,3-TNB (I), 1,2,4-TNB (II) and 1,3,5-TNB (III) have been studied using quantum chemical AM1 method at HF level. The effect of azido substitution on the structures and properties of TNBs has been discussed and the relative stability of the title compounds has been established. The processes of the decomposition of the title compounds by breaking C-NO2, C-N3 and CN-N2 bonds are investigated at UHF-AM1 level. It is shown that the decomposition of the title compounds may be initiated by the cleavage of both C-NO2 and N-N2 bonds.展开更多
Using two structurally related benzoates bearing different H-bond acceptors as co-ligands, three new azido-CuⅡ compounds, [Cu(L1)(N3)(H2O)]n (1), [Cu(L1)(N3)(MeOH)]n (2), and [CuL2HL2(N3)3(H2O)]n (3) (HL1 = 4-nitrobe...Using two structurally related benzoates bearing different H-bond acceptors as co-ligands, three new azido-CuⅡ compounds, [Cu(L1)(N3)(H2O)]n (1), [Cu(L1)(N3)(MeOH)]n (2), and [CuL2HL2(N3)3(H2O)]n (3) (HL1 = 4-nitrobenzoic acid; HL2 = 2-phenyl-4-quinolinecarboxylic acid), have been synthesized and structurally characterized. 1 is a carboxylate/EO-azido bridged copper chain, forming 3D structure by H-bonds, and 2 has a similar chain structure as 1 but forming a 2D structure by H-bonds, while 3 is a 3D supramolecular network with ternary center H-bonds. Magnetic study indicates that domain ferromagnetic coupling interactions were found to exist in complexes 1 and 3.展开更多
文摘New highly stereoregular 2, 3 -di- O-(p-azidobenzyl )-(1 →5 ) - α-D -ribofuranan was synthesized byselective ring-opening polymerization of 1, 4-anhydro-2, 3 - di-O -(p-azidobenzyl )-α-D -ribopyranose(ADABR) using phosphorus pentafluoride or tin tetrachloride as catalyst at low temperature indichloromethane. The monomer was obtained by the reaction of p - bromomethyl -phenyleneazide with 1, 4 -anhydro-α-D-ribose in DMF. The structure of poly(ADANR) was identified by specific rotation and ^(13)C-NMR spectroscopy. Acid chloride-AgCl_4 complex catalyst such as CH_2=C(CH_3)C^+OClO_4^- used in thepolymerization resulted in polymers with mixed structures, i.e. (1→5)-α-D-ribofuranosidic and (1→4)-β-D-ribopyranosidic units. However, with C_6H_5C^+OClO_4^- as catalyst, pure (1→5)-α-D-ribofuranan was obtained.The effects of catalyst, polymerization temperature and time on polymer stereoregularity were examined, andthe mechanism of the ring-opening polymerization was discussed.
文摘The complex [Ni(L)(N3)2](H_2O (L=N,N(-Bis(2-pyridylaldehyde) condensation 1,3-diaminopropane) was synthesized by the reaction of NiCl2(6H_2O with 2-pyridylaldehyde and 1,3-diaminopropane and sodium azide in the ethanol. A single-crystal X-ray study shows that the complex is a six-coordinated nickel (II) with an octahedral environment compound (C15H18N10NiO). The crystal is orthogonal, space group Pbca, with unit cell parameters: a = 13.577(3), b = 15.261(3), c = 17.554(4) ?, V= 3637(1) ?3, Z=8, Mr=413.10, Dc=1.509 g/cm3, ( = 1.096 mm－1, F(000) = 1712, T = 293(2)K, R = 0.0411, wR = 0.1048 for 2888 reflections with I >2( (I). The distances between Ni and N atoms (N(1), N(2), N(3), N(4)) range from 2.050(2) to 2.140(2)?. The distances of Ni-N(5) and Ni-N(8) are 2.115(3) and 2.133(3)?, respectively. The solvent molecule H_2O(O(1)) is linked by hydrogen bonds with O(1) and N(5) and N(8) atoms. Their distances are 2.881(+x, +y, +z) and 2.893(0.5+x, y, 0.5+z)?, respectively.
基金the National Natural Science Foundation of China for financial support.(Grant Nos.20072018 and 20372039).
文摘A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts of stable, non-radioactive labeled DNA and RNA hybridization probes. And it is supposed to be easily detected for its photochromic properties.
基金supported by NNSFC (21231003, 20972023, 21076037)
文摘A new thiolate-bridged diiron complex with two mono-coordinated azido ligands, [Cp＊Fe（kt-SMe）N3]2 （Cp^＊ = η^5-C5Me5）, was synthesized from [Cp＊Fe（η-SMe）MeCNMPF6]2 and NaN3 in a bi-solvent system of acetone and methanol. X-ray crystal structural analysis shows that the compound belongs to the orthorhombic Fdd2 space group, with a = 14.3771（15）, b = 71.424（8）, c = 9.7010（10）A, V = 9961.7（18） A3, C22H36Fe2N6S2, Mr = 560.39, Dc = 1.495 g/cm^3, F（000） = 4704,μ（MoKa） = 1.355 mm-I and Z = 16. The compound consists ofa di（u-thiolate）diiron unit {Cp＊Fe（p-SMe）}2, in which each iron is coordinated by a terminal azido ligand. Magnetic characterizations show spin canting behavior for the title compound.
基金Supported by the National Natural Science Foundation of China(No.20771083)
文摘The organic-inorganic hybrid complex with formula [（CuL）2Cu3（μ-1,1-N3）4（ClO4）2], complex 1, {CuL, [5,6：14,l5-dibenzo-1,4,8,12-tetraazacyclopentadeca-7,3-diene-2,3-dione（2-）]copper（Ⅱ）}, has been synthesized and structurally determined. The crystals of complex 1 crystallize in the triclinic system with space group P1, a=0.92983（12） nm, b=1.09644（14） nm, c=1.27396（16） nm, α=70.782（2）°β=86.266（2）°,γ=78.284（2）°. In this complex, the five copper ions are bridged by macrocyclic oxamide groups and azido. Furthermore, C-H…O hydrogen bond interactions link the pentanuclear fragments to form a 2D supramolecular architecture.
基金Project 29932020 was supported by the National Natural Science Foundation of China.
文摘Poly[styrene(iodosodiacetate)] reacted with diaryl diselenides, followed by sodium azide, giving 1-azido-2-arylselenoalkanes regioselectively. The polymer reagent could be regenerated and reused.
文摘The 1-azido-2-chloro-4-nitrobenzene was prepared by nucleophilic substitution between 2-chloro-4-nitro-1-(trifluoromethylsulfinyl)benzene and sodium azide, and its structure was characterized by NMR spectrum and X-ray single-crystal diffraction. It crystallizes in the monoclinic system, space group P21/n, Z = 8 and Mr = 198.57. A cultivation process of the single crystal of unstable aryl azide was provided. The group of trifluoromethyl sulfinyl was found for the first time to be a new excellent leaving group of aromatic nucleophilic substitution reactions.
基金This work was supported by the National Natural Science Foundation of China(Grant Nos.20071019 and 90101028).
文摘A novel one-dimensional manganese(II) complex containing nitronyl nitroxide radical [Mn2(IM2-py)2(Ac)2(μ1,1-N3)(μ1,3-N3)·EtOH]n was synthesized and characterized structurally and magnetically. It crystallizes in the monoclinic space group p21/n. Each Mn(II) ion is six-coordinated in a distorted octahedral environment. The two N atoms of the nitronyl nitroxide radical and the two O atoms of acetate ligands are in the equatorial plane, whereas the two different azido bridging ligands are in trans axial position. Mn(II) ions are linked by nitrogen atom of μ1,1-azido and oxygen atoms of two carboxy groups to form a Mn-Mn unit. Mn-Mn units are linked by azido ligands through μ1,3 bridging style to form a one-dimensional chain. The compound is connected by the coordination bonds, π-π interactions and hydrogen bonds as a three-dimensional structure. Magnetic susceptibility data support that there are stronger antiferromagnetic interactions between the radical and Mn(II) ion, weak antiferromagnetic interactions between the Mn-R units, and very weak antiferromagnetic interactions between the R-Mn-Mn-R units.
基金supported by MOE Innovation Team of China(No.IRT13022)
文摘A coordination polymer formulated as {[Mn2L（N3）4]·2H2O）n（1） [L = 1,4-bis（pyridinil-3-carboxylato）-1,4- dimethylbenzene] was synthesized and structurally and magnetically characterized. The uniform Mn（Ⅱ） chains with mixed （μ-EO-N3）2（μ-COO） triple bridges （EO = end-on） are linked by L ligands to generate a 2-fold interpenetrating 3D framework. Meanwhile, magnetism analysis reveals antiferromagnetic coupling for 1.
文摘2-Azido-4-nitroimidazole and its derivatives have been synthesized for energetic material applications. The synthesized compounds were fully characterized by 1H, 13C NMR spectroscopy and elemental analysis. Most of them were determined by single crystal X-ray diffraction. The calculated densities of the compounds range between 1.71 and 1.92 g,cm-3. The calculated detonation pressures （P） for these derivatives fall in the range of 25.17 to 32.62 GPa and the detonation velocities （D） are distributed from 7.65 to 8.55 km·s-1.
文摘The 2-azido-4-nitroimidazole-based energetic salts were synthesized in a simple and straightforward manner. The structures of these new salts were determined by IR, 1H NMR and 13C NMR spectroscopy and elemental analysis. These salts also exhibited high positive enthalpies of formation, high nitrogen content, and moderate detonation properties.
基金the National Natural Science Foundation of China(21871043)the Department of Science and Technology of Jilin Province(20180101185JC,20190701012GH)the Fundamental Research Funds for the Central Universities(2412019ZD001).
文摘The development of azide migration reactions is a formidable challenge due to potential competition from side processes driven by the release of molecular nitrogen. Here, we show a novel neighbouring carbonyl group-assisted sequential 1,2-azide and 1,4-oxygen migration reaction of α-vinyl azides for the efficient preparation of a range of α-azido ketones. This represents the first transformation of α-vinyl azides into α-azido ketones. Notable features of this method are its high efficiency, broad substrate scope, excellent functional group compatibility, and high yields. The computational studies gave a key insights into the regioselective 1,2-azide and 1,4-oxygen migrations assisted by the neighbouring carbonyl group. Further conversions into a variety of nitrogen-containing compounds demonstrated the synthetic utility of the α-azido ketone products. Preliminary mechanistic studies disclosed a novel reaction mechanism involving neighbouring carbonyl group-assisted sequential 1,2-azide and1,4-oxygen migrations.
基金Project (No. 960539) supported by the Natural Science Foundation of China Academy of Engineering Physics
文摘The geometries, heats of formation and electronic structures of 15 azido-derivatives of 1,2,3-TNB (I), 1,2,4-TNB (II) and 1,3,5-TNB (III) have been studied using quantum chemical AM1 method at HF level. The effect of azido substitution on the structures and properties of TNBs has been discussed and the relative stability of the title compounds has been established. The processes of the decomposition of the title compounds by breaking C-NO2, C-N3 and CN-N2 bonds are investigated at UHF-AM1 level. It is shown that the decomposition of the title compounds may be initiated by the cleavage of both C-NO2 and N-N2 bonds.
基金Supported by the Major State Basic Research Development Program of China (Grant No. 2007CB815305)National Natural Science Foundation of China (Grant No. 50673043, 20773068)Natural Science Foundation of Tianjin (Grant No. 07- JCZDJC00500)
文摘Using two structurally related benzoates bearing different H-bond acceptors as co-ligands, three new azido-CuⅡ compounds, [Cu(L1)(N3)(H2O)]n (1), [Cu(L1)(N3)(MeOH)]n (2), and [CuL2HL2(N3)3(H2O)]n (3) (HL1 = 4-nitrobenzoic acid; HL2 = 2-phenyl-4-quinolinecarboxylic acid), have been synthesized and structurally characterized. 1 is a carboxylate/EO-azido bridged copper chain, forming 3D structure by H-bonds, and 2 has a similar chain structure as 1 but forming a 2D structure by H-bonds, while 3 is a 3D supramolecular network with ternary center H-bonds. Magnetic study indicates that domain ferromagnetic coupling interactions were found to exist in complexes 1 and 3.
