期刊文献+
共找到10篇文章
< 1 >
每页显示 20 50 100
Synthesis and Molecular Structure of a C-iso-Butyl-cavitand Bowl with Trimethyl and Methylol Groups
1
作者 LIUShu-Qun YAOWen-Rui ZHANGQian-Feng 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第4期444-448,共5页
A C-iso-butyl-cavitand bowl with trimethyl and methylol groups was isolated from the acetoxymethyl hydrolysis of mono-methylbromo-cavitand in THF. The molecular structure of the present cavitand compound was determi... A C-iso-butyl-cavitand bowl with trimethyl and methylol groups was isolated from the acetoxymethyl hydrolysis of mono-methylbromo-cavitand in THF. The molecular structure of the present cavitand compound was determined by single-crystal X-ray diffraction. The compound (C56H70N2O9) crystallizes in orthorhombic, space group Pnma with a = 19.5060(15), b = 19.8136(15), c = 12.9508(10) ?, V = 5005.3(7) ?3, Z = 4, Mr = 915.14, Dc = 1.214 g/cm3, F(000) = 1968, μ = 0.081 mm?1, S = 1.012, the final R = 0.0789 and wR = 0.1488 for 2298 observed reflections with I > 2σ(I) and 322 variable parameters. The structure exhibits a rigid bowl-cavity with an available functional hydroxyl group. The bowl of cavitand contains a CH3CN solvent molecule, and the depth of the bowl-shaped cavity is ca. 2.42 ?. 展开更多
关键词 structure RESORCINARENE cavitand supramolecular chemistr
在线阅读 下载PDF
State-of-the-art and recent progress in resorcinarene-based cavitand
2
作者 Kaiya Wang Qian Liu +3 位作者 Li Zhou Hao Sun Xiaoquan Yao Xiao-Yu Hu 《Chinese Chemical Letters》 SCIE CAS CSCD 2023年第10期27-34,共8页
Compartmentalization in the biological world brings excellent efficiency and specificity to the formation of complex compounds,inspiring supramolecular chemists to continuously search for defined spaces that can mimic... Compartmentalization in the biological world brings excellent efficiency and specificity to the formation of complex compounds,inspiring supramolecular chemists to continuously search for defined spaces that can mimic such natural binding sites.Bowl-shaped cavitands built up from resorcinarenes(RA)present rigid and preorganized concave surfaces,which are capable of mimicking the molecular recognition properties of enzymes.The versatile scaffold of RA endows the cavitand with terrific variety and excellent binding behavior.This review provides a comprehensive overview over the structural modification to date in the high attention field of RA-based cavitands development.Different strategies for synthesizing diverse cavitands,such as small cavity cavitands,wider cavity cavitands,deep cavity cavitands,biscavitands,and asymmetric cavitands,are discussed in details.Furthermore,insights into their applications including catalysis,separations and sensing are provided. 展开更多
关键词 RESORCINARENE cavitand Supramolecular chemistry Host-vip chemistry Molecular recognition
原文传递
Metal coordination to a deep cavitand promotes binding selectivities in water
3
作者 Yong-Qing Chen Hua-Wei Guan +2 位作者 Kuppusamy Kanagaraj Julius Rebek Yang Yu 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第11期4908-4911,共4页
One goal of supramolecular chemistry is the creation of synthetic receptors that have a high affinity for hydrophilic molecules in water.We found that cavitands with upper rims extended by pyridyl groups coax hydrophi... One goal of supramolecular chemistry is the creation of synthetic receptors that have a high affinity for hydrophilic molecules in water.We found that cavitands with upper rims extended by pyridyl groups coax hydrophilic vips into the cavity where they are shielded from the aqueous environment.The ability of Pd(Ⅱ)to coordinate adjacent pyridyl groups leads to increased selectivity for highly hydrophilic solvent molecules such as acetone,1,4-dioxane and tetrahydrofuran in water.Analysis of the binding behavior indicated that metal-coordination restricts the container entrance,shrinks the effective cavity volume and increases the energetic barrier to vip exchange. 展开更多
关键词 Host-vip chemistry Metallo cavitand Hydrophilic small molecules Molecular recognition Water-soluble containers
原文传递
Supramolecular prodrug vesicles for selective antimicrobial therapy employing a chemo-photodynamic strategy
4
作者 Hao Sun Shengke Li +4 位作者 Qian Liu Minzan Zuo Xueqi Tian Kaiya Wang Xiao-Yu Hu 《Chinese Chemical Letters》 2025年第3期267-271,共5页
Supramolecular prodrug vesicles(H-4⊃B-2@MB)with selective antibacterial activity have been successfully constructed.Specifically,a natural antibiotic prodrug(B-2)with glutathione(GSH)-responsiveness was synthesized.Th... Supramolecular prodrug vesicles(H-4⊃B-2@MB)with selective antibacterial activity have been successfully constructed.Specifically,a natural antibiotic prodrug(B-2)with glutathione(GSH)-responsiveness was synthesized.The hydrophobic interaction between B-2 and a novel water-soluble cavitand with deep cavity(H-4)resulted in the formation of a host-vip complex,which further self-assembled into supramolecular vesicles.The formed vesicles could effectively encapsulate the photosensitizer methylene blue(MB),enabling co-delivery of antibiotics and photosensitizers in the presence of GSH.Moreover,upon excitation at 630 nm,the photosensitizers generate reactive oxygen species(ROS),effectively eradicating E.coli through combined chemo-photodynamic therapy.Considering that GSH is predominantly present in Gram-negative bacteria such as E.coli,this strategy exhibits substantial potential for selectively inhibiting bacteria characterized by high GSH levels to regulate bacterial colony equilibrium. 展开更多
关键词 Supramolecular prodrug Selective antibacterial activity Host-vip complex cavitand Combination therapy
原文传递
客体构象自适应驱动的分子胶囊
5
作者 陈永青 高雅 +1 位作者 朱玉洁 于洋 《化学学报》 北大核心 2025年第9期993-999,共7页
非共价分子胶囊是超分子化学的核心研究对象,其基于氢键、静电等非共价作用构建的动态限域结构,在催化、医药及材料等领域极具应用价值.然而,传统分子胶囊的构筑常依赖于超分子主体中预置互补基元.本工作突破这一局限,设计合成以雷锁酚... 非共价分子胶囊是超分子化学的核心研究对象,其基于氢键、静电等非共价作用构建的动态限域结构,在催化、医药及材料等领域极具应用价值.然而,传统分子胶囊的构筑常依赖于超分子主体中预置互补基元.本工作突破这一局限,设计合成以雷锁酚杯[4]芳烃为骨架的水溶性2-氨基苯并咪唑分子杯1,通过客体分子调控柔性片段构象,实现水相中超分子主体二聚.以对称型直链烷烃和非对称型直链烷基苯乙烯类半菁染料为客体,系统探究其与分子杯1的主客体识别行为.结果表明,碳链长度为n=12~20的直链烷烃,分别通过延展、延展/螺旋、延展/盘旋等构象,协同疏水作用诱导分子杯二聚形成胶囊;苯乙烯类半菁染料分子的柔性烷基链,经延展或折叠构象,同样可驱动分子杯二聚.疏水作用与C—H…π作用的协同效应,是该类分子胶囊形成的主要驱动力. 展开更多
关键词 分子杯 构象自适应 疏水作用 C—H…π作用 分子胶囊
原文传递
Shape Selectivity of a Metallo Cavitand Host Allows Separation of n-Alkanes from Isooctane
6
作者 Yun-Hui Wan Faiz-Ur Rahman +1 位作者 Julius Rebek Jr. Yang Yu 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2021年第6期1498-1502,共5页
The use of a metallo cavitand for the selective sequestration of n-alkanes from their mixtures with isooctane is described.Competition experiments and NMR spectroscopy are used to show the preference of a water-solubl... The use of a metallo cavitand for the selective sequestration of n-alkanes from their mixtures with isooctane is described.Competition experiments and NMR spectroscopy are used to show the preference of a water-soluble cavitand host for vips that are hydro-phobic and have narrow or flat shapes.The host showed selectivity for trans 1,4-dimethylcyclohexane over the cis-isomers.The sep-arations of n-alkanes from isooctane by gas/liquid adsorption and a liquid/liquid extraction are detailed. 展开更多
关键词 Metallo cavitand Shape selectivity eceptor Alkane separation Host-vip system
原文传递
类杯芳烃孔穴桥联双芘分子开关化合物 被引量:3
7
作者 徐海 赵斯祺 +3 位作者 任扬 蔡健峰 汪翔 林雨霖 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2015年第12期2421-2426,共6页
利用构型可变的分子开关类杯芳烃孔穴化合物(Cavitand)作为母体,合成了2种具有不同臂长的双芘Cavitand化合物.在室温及中性状态下,2种双芘Cavitand化合物均可检验出分子内激基复合物荧光,其中短臂双芘Cavitand化合物的荧光明显强于长臂C... 利用构型可变的分子开关类杯芳烃孔穴化合物(Cavitand)作为母体,合成了2种具有不同臂长的双芘Cavitand化合物.在室温及中性状态下,2种双芘Cavitand化合物均可检验出分子内激基复合物荧光,其中短臂双芘Cavitand化合物的荧光明显强于长臂Cavitand化合物.经三氟乙酸酸化后,2种双芘化合物的分子内激基复合物荧光消失;而继续使用碱中和至中性,则荧光恢复.这个荧光出现-消失-出现的过程验证了Cavitand母体化合物分子构型闭合-打开-闭合可有效调控分子激基复合物荧光开关过程.此外,通过高斯计算模拟了2种化合物的理论分子构型,发现长臂双芘化合物在Cavitand母体构型处于闭合状态时2个芘基团重叠部分较少是其分子内激基复合物荧光较弱的关键原因. 展开更多
关键词 分子开关 类杯芳烃孔穴化合物 荧光 双芘cavitand化合物
在线阅读 下载PDF
C-H…X-C bonds in alkyl halides drive reverse selectivities in confined spaces
8
作者 Manuel Petroselli Yong-Qing Chen +2 位作者 Ming-Kai Zhao Julius Rebek Jr. Yang Yu 《Chinese Chemical Letters》 SCIE CAS CSCD 2023年第5期237-240,共4页
Binding of non-activated alkyl halides(2-20)in water-soluble cavitand(1)through supramolecular forces is here reported,with emphasis on the role of size and polarizability of the halogen atom in the formation of intra... Binding of non-activated alkyl halides(2-20)in water-soluble cavitand(1)through supramolecular forces is here reported,with emphasis on the role of size and polarizability of the halogen atom in the formation of intramolecular C-H hydrogen bonds in confined spaces.Rare reverse affinity in water(RI<RBr<RCl)is surprisingly observed for the more water-soluble short alkyl halides in dynamic open-ended containers.Competitive bindings and theoretical calculations confirm the unusual selectivity and the presence of C-H hydrogen bonds in non-activated systems for the first time,pointing out the importance and effect of subtle forces on molecular recognition in confined spaces. 展开更多
关键词 Water-soluble cavitand Host-vip complex Molecular recognition C-H hydrogen bond Alkyl halides
原文传递
Synthesis and Structure of a Host-vip Inclusion System between C-propyl-o-toluidine-methyl-resorcin[4]arene and Ethanol Solvate
9
作者 Lusi Chen Rurou Jiang +2 位作者 Huatian Shi Aiquan Jia Qianfeng Zhang 《Journal of Materials Science and Chemical Engineering》 2023年第12期22-33,共12页
Tetra-bromo-methyl-resorcin[4]arene cavitands were synthesized and C-2 position amine functionalized to obtain C-propyl-o-toluidine-methyl-resorcin[4]arene cavitand 4, and the crystal containing one solvate molecule o... Tetra-bromo-methyl-resorcin[4]arene cavitands were synthesized and C-2 position amine functionalized to obtain C-propyl-o-toluidine-methyl-resorcin[4]arene cavitand 4, and the crystal containing one solvate molecule of ethanol was obtained in a dichloromethane-ethanol solvent system, its structure crystallized in the monoclinic space group P2<sub>1</sub>/n, with a = 12.521(3) Å, b = 21.738(6) Å, c = 25.353(6) Å, α = 90˚, β = 102.372(4)˚, γ = 90˚, and Z = 4. The compound was determined by single-crystal X-ray diffraction and characterized by <sup>1</sup>H NMR, FT-IR and elemental analyses. 展开更多
关键词 arene cavitand Amine Functionalized Dichloromethane-Ethanol
在线阅读 下载PDF
巨型给-受体分子开关化合物的合成及性质研究
10
作者 眭玉光 周锦荣 +2 位作者 廖攀 梁文杰 徐海 《化学学报》 SCIE CAS CSCD 北大核心 2022年第8期1061-1065,共5页
以构象可变的间苯二酚杯[4]芳烃孔穴化合物(Cavitand)为分子开关母体,合成了一种新颖的给-受体(D-A)型分子开关化合物(化合物1),该分子是目前已知分子量最大的D-A型间苯二酚杯[4]芳烃Cavitand(分子量为3064.9966).其中,以卟啉为给体,富... 以构象可变的间苯二酚杯[4]芳烃孔穴化合物(Cavitand)为分子开关母体,合成了一种新颖的给-受体(D-A)型分子开关化合物(化合物1),该分子是目前已知分子量最大的D-A型间苯二酚杯[4]芳烃Cavitand(分子量为3064.9966).其中,以卟啉为给体,富勒烯为受体.在pH诱导下,化合物1可发生构象变化,即由原来的关闭状(vase)转为打开状(kite);而在降低温度和引入Zn^(2+)的条件下,不能促使化合物1发生构象变化.p H诱导构象发生变化的原因,是酸的加入会导致喹喔啉手臂上的N原子发生质子化,从而使得形成的静电排斥作用促使手臂之间相互远离.此外,对化合物1的光物理性质研究表明,存在卟啉向富勒烯的单线态能量转移,其单线态能量转移速率常数为1.1×10^(7)s^(-1),单线态能量转移效率为9.63%. 展开更多
关键词 分子开关 给-受体 卟啉-富勒烯 芳烃孔穴化合物 能量转移
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部