蛋白质泛素化修饰广泛参与植物的生长发育及逆境胁迫响应,其中RING-finger型E3泛素连接酶基因salt and drought induced ring finger1(SDIR1)在植物抗逆中具有重要的作用.为了解茶树SDIR1(CsSDIR1)在抗逆应答中的作用机制,采用RT-PCR技...蛋白质泛素化修饰广泛参与植物的生长发育及逆境胁迫响应,其中RING-finger型E3泛素连接酶基因salt and drought induced ring finger1(SDIR1)在植物抗逆中具有重要的作用.为了解茶树SDIR1(CsSDIR1)在抗逆应答中的作用机制,采用RT-PCR技术从茶树中克隆CsSDIR1的全长cDNA序列及启动子序列,对其生物信息学特征进行分析,并采用qRT-PCR技术检测该基因的组织表达特异性及在不同逆境胁迫下的表达模式.结果显示,CsSDIR1基因的开放阅读框(ORF)长831 bp,编码276个氨基酸,蛋白质分子量(Mr)为30.085×103,理论等电点为6.54;氨基酸序列分析表明,CsSDIR1属于疏水性蛋白、定位在胞内膜上,与其他植物中的SDIR1相似性较高,在其N-端和C-端分别含有2个保守的跨膜结构域和C3H2C3 RING finger功能域;CsSDIR1与猕猴桃关系最近. CsSDIR1上游启动子含多个与干旱胁迫和盐胁迫响应相关的元件.表达分析显示,CsSDIR1在茎中的表达量显著高于根、叶和花;ABA、干旱和高盐诱导其表达,低温抑制CsSDIR1的表达.根据上述结果推测CsSDIR1基因可能参与了茶树的抗逆响应.展开更多
后量子时代,基于格理论的公钥密码被认为是最有前途的抵抗量子计算机攻击的公钥密码体制.然而,相对于格上公钥加密体制和数字签名方案的快速发展,基于格上困难问题的密钥协商协议成果却较少.因此,现阶段如何构建格上安全的密钥协商协议...后量子时代,基于格理论的公钥密码被认为是最有前途的抵抗量子计算机攻击的公钥密码体制.然而,相对于格上公钥加密体制和数字签名方案的快速发展,基于格上困难问题的密钥协商协议成果却较少.因此,现阶段如何构建格上安全的密钥协商协议是密码学领域具有挑战性的问题之一.针对上述问题,基于环上带错误学习问题困难假设,采用调和技术构造了一种新的认证密钥协商协议RAKA(authenticated key agreement protocol based on reconciliation technique),该方案采用格上陷门函数技术提供了单向认证功能,并且在Ring-LWE假设下证明是安全的.与现有的基于LWE的密钥协商协议相比,该方案的共享会话密钥减小为2nlog q,效率更高;同时,由于该方案的安全性是基于格上困难问题,因此可以抵抗量子攻击.展开更多
Nano-ring-type magnetic tunnel junctions （NR-MTJs） with the layer structure of Ta（5）/Ir22Mn78（10）/ Co75Fe25（2）/Ru（0.75）/CoooFe20B20（3）/Al（0.6）-oxide/Co60Fe20B20（2.5）/Ta（3）/Ru（5） （thickness unit：...Nano-ring-type magnetic tunnel junctions （NR-MTJs） with the layer structure of Ta（5）/Ir22Mn78（10）/ Co75Fe25（2）/Ru（0.75）/CoooFe20B20（3）/Al（0.6）-oxide/Co60Fe20B20（2.5）/Ta（3）/Ru（5） （thickness unit： nm） were nano-fabricated on the Si（100）/SiO2 substrate using magnetron sputtering deposition combined with the optical lithography, electron beam lithography （EBL） and Ar ion-beam etching techniques. The smaller NR-MTJs with the inner- and outer-diameter of around 50 and 100 nm and also their corresponding NR-MTJ arrays were nano-patterned. The tunnelling magnetoresistance （TMR ＆ R） versus driving current （I） loops for a spin-polarized current switching were measured, and the TMR ratio of around 35% at room temperature were observed. The critical values of switching current for the free Co60Fe20B20 layer relative to the reference Co6oFe2oB2o layer between parallel and anti-parallel magnetization states were between 0.50 and 0.75 mA in such NR-MTJs. It is suggested that the applicable MRAM fabrication with the density and capacity higher than 256 Mbit/inch2 even 6 Gbite/inch2 are possible using both I NR-MTJ＋1 transistor structure and current switching mechanism based on based on our fabricated 4×4 MRAM demo devices.展开更多
Highly potent ionic organocatalyst is developed for room-temperature controlled ring-opening polymerization(ROP)of lactones,includingδ-valerolactone,ε-caprolactone,andδ-hexalactone.The catalysts are prepared by sim...Highly potent ionic organocatalyst is developed for room-temperature controlled ring-opening polymerization(ROP)of lactones,includingδ-valerolactone,ε-caprolactone,andδ-hexalactone.The catalysts are prepared by simply mixing tetra-n-butyl ammonium hydroxide and a(thio)urea at elevated temperature under vacuum,and used in cooperation with an alcoholic initiator.The performance of the catalyst is readily adjusted and optimized through variation of the(thio)urea precursor,catalyst composition,and reaction condition.Urea-derived catalysts are generally superior to thiourea-derived ones.Provided with proper N-substituents,the catalyst affords both high polymerization efficiency and high selectivity for monomer enchainment over macromolecular transesterification,even at high monomer conversion and/or substantially extended reaction time.In addition to acidity,structural symmetry of the urea also proves decisive for the catalytic activity,which enables a catalyst-assisted proton transfer process for the ring-opening of lactone and thus provides a novel mechanistic insight for ROP catalyzed by hydrogen-bonding type bifunctional ionic organocatalysts.展开更多
Star-branched polyamide 6 was prepared via anionic ring-opening polymerization of ε-caprolactam in the presence of a simple benzene-centered trifunctional activator of N,N＇,N＂-trimesoyltricaprolactam. A high polyme...Star-branched polyamide 6 was prepared via anionic ring-opening polymerization of ε-caprolactam in the presence of a simple benzene-centered trifunctional activator of N,N＇,N＂-trimesoyltricaprolactam. A high polymer yields of above 95% were achieved at 160 ℃ for 15 min utilizing ε-caprolactam magnesium bromide as a catalyst. Compared with its linear counterpart, the resultant star-branched polyamide 6 showed smaller relative viscosity （1.51 ）, decreased melting temperature （218 ℃） and lower crystallinity （24.2%）. The specific properties demonstrated the existence of a star-branched structure and provided potential advantages in engineering applications.展开更多
From the general formula for calculating the efficiency of planetary geartrains, the efficiency of the double crank ring-plate-type pin-cycloidal gear planetary drive isderived. To prove the theory, an experimental st...From the general formula for calculating the efficiency of planetary geartrains, the efficiency of the double crank ring-plate-type pin-cycloidal gear planetary drive isderived. To prove the theory, an experimental study has been conducted. The tested value of theefficiency of a sample set of the new-type drive in the experiment agrees with the calculated one.It shows that the new-type drive is of not merely high bearing capacity, but also quite highefficiency.展开更多
A series of zinc silylamido complexes based upon NNO tridentate enolic Schiff base framework have been synthesized and characterized. These complexes were tested for the ring opening polymerization of lactide and e-ca...A series of zinc silylamido complexes based upon NNO tridentate enolic Schiff base framework have been synthesized and characterized. These complexes were tested for the ring opening polymerization of lactide and e-caprolactone, exhibiting notably high activity at ambient temperature, The influence of imine bridge length and substituents of diketone over the course of polymerization was investigated in details. Remarkably, 4a was confirmed to be a rare example of exceedingly active and robust zinc catalysts, achieving major transformation of lactide under extremely low loading （0.025 mol%） within 18 rain. The influence of various monomers as well as the polymerization mechanism have also been discussed.展开更多
In this paper,ring-opening polymerization of trimethylene carbonate(TMC)with rare earth(Nd,Y,La)ρ-tert- butylcalix[n]arene(n=4,6,and 8)complexes as catalysts has been studied.Poly(trimethylene carbonate)(PTMC)with M_...In this paper,ring-opening polymerization of trimethylene carbonate(TMC)with rare earth(Nd,Y,La)ρ-tert- butylcalix[n]arene(n=4,6,and 8)complexes as catalysts has been studied.Poly(trimethylene carbonate)(PTMC)with M_v of 21,400 was produced by bulk polymerization under the conditions as follows:[TMC]_0/[Nd](molar ratio)=1000,80℃, 8 h.Mechanism study reveals that the polymerization proceeds via a coordination mechanism.展开更多
The ring-opening polymerization of e-caprolactone (CL) initiated by novel single lanthanide tris(4-tert-butylphenolate)s [Ln(OTBP)3] is reported. Single-component La(OTBP)3 can effectively prepare polycaprolactone (PC...The ring-opening polymerization of e-caprolactone (CL) initiated by novel single lanthanide tris(4-tert-butylphenolate)s [Ln(OTBP)3] is reported. Single-component La(OTBP)3 can effectively prepare polycaprolactone (PCL) with over 90% yield and viscosity average molecular weight about 60 x 10 under quite mild conditions: molar ratio of CL to initiator is 1000, 60 C, 2 h in toluene. Mechanism study indicates that the monomer inserts into the growing chain via the break of acyl-oxygen bond of CL.展开更多
A series of cyclic (arylene phosphonate) oligomers were prepared by reaction of phenylphosphonic dichloride (PPD) with various bisphenols under pseudo-high dilution conditions via interfacial polycondensation. The yie...A series of cyclic (arylene phosphonate) oligomers were prepared by reaction of phenylphosphonic dichloride (PPD) with various bisphenols under pseudo-high dilution conditions via interfacial polycondensation. The yield of cyclic (arylene phosphonate) oligomers is over 85% by using hexadecyltrimethylammoniun bromide as phase transfer catalyst (PTC) at 0 'C . The structures of the cyclic oligomers were confirmed by a combination of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and IR analysis. These cyclic oligomers undergo facile ring-opening polymerization in the melt by using potassium 4,4'-biphenoxide as the initiator to give linear polyphosphonate. Free-radical ring-opening polymerization of cyclic(arylene phosphonate) oligomers containing sulfur linkages was also performed in the melt using 2,2'-dithiobis(benzothiazole) (DTB) as the initiator at 270 °C and the resulting polymer had a Mw, of 8 × 103 with a molecular weight distribution of 4. Ring-opening copolymerization of these cyclic oligomers with cyclic carbonate oligomers was also achieved. The average molecular weight of the resulting copolymer is higher than the corresponding homopolymer and the thermal stability of the copolymer is better than the corresponding homopolymer.展开更多
文摘蛋白质泛素化修饰广泛参与植物的生长发育及逆境胁迫响应,其中RING-finger型E3泛素连接酶基因salt and drought induced ring finger1(SDIR1)在植物抗逆中具有重要的作用.为了解茶树SDIR1(CsSDIR1)在抗逆应答中的作用机制,采用RT-PCR技术从茶树中克隆CsSDIR1的全长cDNA序列及启动子序列,对其生物信息学特征进行分析,并采用qRT-PCR技术检测该基因的组织表达特异性及在不同逆境胁迫下的表达模式.结果显示,CsSDIR1基因的开放阅读框(ORF)长831 bp,编码276个氨基酸,蛋白质分子量(Mr)为30.085×103,理论等电点为6.54;氨基酸序列分析表明,CsSDIR1属于疏水性蛋白、定位在胞内膜上,与其他植物中的SDIR1相似性较高,在其N-端和C-端分别含有2个保守的跨膜结构域和C3H2C3 RING finger功能域;CsSDIR1与猕猴桃关系最近. CsSDIR1上游启动子含多个与干旱胁迫和盐胁迫响应相关的元件.表达分析显示,CsSDIR1在茎中的表达量显著高于根、叶和花;ABA、干旱和高盐诱导其表达,低温抑制CsSDIR1的表达.根据上述结果推测CsSDIR1基因可能参与了茶树的抗逆响应.
文摘后量子时代,基于格理论的公钥密码被认为是最有前途的抵抗量子计算机攻击的公钥密码体制.然而,相对于格上公钥加密体制和数字签名方案的快速发展,基于格上困难问题的密钥协商协议成果却较少.因此,现阶段如何构建格上安全的密钥协商协议是密码学领域具有挑战性的问题之一.针对上述问题,基于环上带错误学习问题困难假设,采用调和技术构造了一种新的认证密钥协商协议RAKA(authenticated key agreement protocol based on reconciliation technique),该方案采用格上陷门函数技术提供了单向认证功能,并且在Ring-LWE假设下证明是安全的.与现有的基于LWE的密钥协商协议相比,该方案的共享会话密钥减小为2nlog q,效率更高;同时,由于该方案的安全性是基于格上困难问题,因此可以抵抗量子攻击.
基金the State Key Project of Fundamental Research of Ministry of Science and Technology （No. 2006CB932200） the National Natural Science Foundation of China （NSFC, No. 10574156）+2 种基金 the Knowledge Innovation Program of Chinese Aca.demy of Sciencesthe protial support of 0utstanding Young Researcher Foundation （Nos. 50325104 and 50528101） K.C.Wong Education Foundation, Hong Kong.
文摘Nano-ring-type magnetic tunnel junctions （NR-MTJs） with the layer structure of Ta（5）/Ir22Mn78（10）/ Co75Fe25（2）/Ru（0.75）/CoooFe20B20（3）/Al（0.6）-oxide/Co60Fe20B20（2.5）/Ta（3）/Ru（5） （thickness unit： nm） were nano-fabricated on the Si（100）/SiO2 substrate using magnetron sputtering deposition combined with the optical lithography, electron beam lithography （EBL） and Ar ion-beam etching techniques. The smaller NR-MTJs with the inner- and outer-diameter of around 50 and 100 nm and also their corresponding NR-MTJ arrays were nano-patterned. The tunnelling magnetoresistance （TMR ＆ R） versus driving current （I） loops for a spin-polarized current switching were measured, and the TMR ratio of around 35% at room temperature were observed. The critical values of switching current for the free Co60Fe20B20 layer relative to the reference Co6oFe2oB2o layer between parallel and anti-parallel magnetization states were between 0.50 and 0.75 mA in such NR-MTJs. It is suggested that the applicable MRAM fabrication with the density and capacity higher than 256 Mbit/inch2 even 6 Gbite/inch2 are possible using both I NR-MTJ＋1 transistor structure and current switching mechanism based on based on our fabricated 4×4 MRAM demo devices.
基金financially supported by the National Natural Science Foundation of China (Nos. 21734004 and 21674038)
文摘Highly potent ionic organocatalyst is developed for room-temperature controlled ring-opening polymerization(ROP)of lactones,includingδ-valerolactone,ε-caprolactone,andδ-hexalactone.The catalysts are prepared by simply mixing tetra-n-butyl ammonium hydroxide and a(thio)urea at elevated temperature under vacuum,and used in cooperation with an alcoholic initiator.The performance of the catalyst is readily adjusted and optimized through variation of the(thio)urea precursor,catalyst composition,and reaction condition.Urea-derived catalysts are generally superior to thiourea-derived ones.Provided with proper N-substituents,the catalyst affords both high polymerization efficiency and high selectivity for monomer enchainment over macromolecular transesterification,even at high monomer conversion and/or substantially extended reaction time.In addition to acidity,structural symmetry of the urea also proves decisive for the catalytic activity,which enables a catalyst-assisted proton transfer process for the ring-opening of lactone and thus provides a novel mechanistic insight for ROP catalyzed by hydrogen-bonding type bifunctional ionic organocatalysts.
基金supported by a grant from the National High Technology Research and Development Program of China(No.2014AA021201)the National Basic Research Program of China(No.2012CB721104)+1 种基金China Postdoctoral Science Foundation(No.2014M551574)the Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘Star-branched polyamide 6 was prepared via anionic ring-opening polymerization of ε-caprolactam in the presence of a simple benzene-centered trifunctional activator of N,N＇,N＂-trimesoyltricaprolactam. A high polymer yields of above 95% were achieved at 160 ℃ for 15 min utilizing ε-caprolactam magnesium bromide as a catalyst. Compared with its linear counterpart, the resultant star-branched polyamide 6 showed smaller relative viscosity （1.51 ）, decreased melting temperature （218 ℃） and lower crystallinity （24.2%）. The specific properties demonstrated the existence of a star-branched structure and provided potential advantages in engineering applications.
基金This project is supported by National Natural Science Foundation of China (No.50175011).
文摘From the general formula for calculating the efficiency of planetary geartrains, the efficiency of the double crank ring-plate-type pin-cycloidal gear planetary drive isderived. To prove the theory, an experimental study has been conducted. The tested value of theefficiency of a sample set of the new-type drive in the experiment agrees with the calculated one.It shows that the new-type drive is of not merely high bearing capacity, but also quite highefficiency.
基金financially supported by the National Natural Science Foundation of China(Nos.21574124,51503203 and51233004)
文摘A series of zinc silylamido complexes based upon NNO tridentate enolic Schiff base framework have been synthesized and characterized. These complexes were tested for the ring opening polymerization of lactide and e-caprolactone, exhibiting notably high activity at ambient temperature, The influence of imine bridge length and substituents of diketone over the course of polymerization was investigated in details. Remarkably, 4a was confirmed to be a rare example of exceedingly active and robust zinc catalysts, achieving major transformation of lactide under extremely low loading （0.025 mol%） within 18 rain. The influence of various monomers as well as the polymerization mechanism have also been discussed.
基金This work was financially supported by the Special Fund for Major State Basic Research Project(G1999064801)the National Natural Science Foundation of China(Nos.20174033 and 20434020)
文摘In this paper,ring-opening polymerization of trimethylene carbonate(TMC)with rare earth(Nd,Y,La)ρ-tert- butylcalix[n]arene(n=4,6,and 8)complexes as catalysts has been studied.Poly(trimethylene carbonate)(PTMC)with M_v of 21,400 was produced by bulk polymerization under the conditions as follows:[TMC]_0/[Nd](molar ratio)=1000,80℃, 8 h.Mechanism study reveals that the polymerization proceeds via a coordination mechanism.
基金supported by the National Natural Science Foundation of China.(Grant No.20174033 and 20254001)the Special Found for Major State Basic Research Project(Grant No.G1999064801)the Committee of Science and Technology of Zhejiang Province.
文摘The ring-opening polymerization of e-caprolactone (CL) initiated by novel single lanthanide tris(4-tert-butylphenolate)s [Ln(OTBP)3] is reported. Single-component La(OTBP)3 can effectively prepare polycaprolactone (PCL) with over 90% yield and viscosity average molecular weight about 60 x 10 under quite mild conditions: molar ratio of CL to initiator is 1000, 60 C, 2 h in toluene. Mechanism study indicates that the monomer inserts into the growing chain via the break of acyl-oxygen bond of CL.
基金This project was supported by the National Natural Science Foundation of China (No. 20084001).
文摘A series of cyclic (arylene phosphonate) oligomers were prepared by reaction of phenylphosphonic dichloride (PPD) with various bisphenols under pseudo-high dilution conditions via interfacial polycondensation. The yield of cyclic (arylene phosphonate) oligomers is over 85% by using hexadecyltrimethylammoniun bromide as phase transfer catalyst (PTC) at 0 'C . The structures of the cyclic oligomers were confirmed by a combination of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and IR analysis. These cyclic oligomers undergo facile ring-opening polymerization in the melt by using potassium 4,4'-biphenoxide as the initiator to give linear polyphosphonate. Free-radical ring-opening polymerization of cyclic(arylene phosphonate) oligomers containing sulfur linkages was also performed in the melt using 2,2'-dithiobis(benzothiazole) (DTB) as the initiator at 270 °C and the resulting polymer had a Mw, of 8 × 103 with a molecular weight distribution of 4. Ring-opening copolymerization of these cyclic oligomers with cyclic carbonate oligomers was also achieved. The average molecular weight of the resulting copolymer is higher than the corresponding homopolymer and the thermal stability of the copolymer is better than the corresponding homopolymer.
