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1.
LIU Xiang LIU Yu-Jie ZHANG Qian-Feng 《结构化学》2005,24(8):952-956
1 INTRODUCTION Resorcin[4]arene is a cyclic tetramer and can be easily obtained by acid-catalyzed condensation of resorcinol with a variety of aldehydes. The all-cis isomer with crown C4v symmetry is mostly isolated by means of alkyl aldehydes[1]. They have been used as starting materials for the synthesis of cavitands, velc-rands, and even more complex compounds like carce-rands, hemicarceracnds, and holands[2~4]. Of the ob-vious places for the chemical modification of reso-rcin[4]arene… 相似文献
2.
A key feature of resorcin[4]arene cavitands is their ability to switch between a closed/contracted (Vase ) and an open/expanded (Kite ) conformation. The mechanism and dynamics of this interconversion remains, however, elusive. In the present study, the Vase ‐Kite transitions of a quinoxaline‐based and of a dinitrobenzene‐based resorcin[4]arene are investigated using molecular dynamics (MD) simulations in three environments (vacuum, chloroform, and toluene) and at three temperatures (198.15, 248.15, and 298.15 K). The challenge of sampling the Vase ‐Kite transition, which occurs experimentally on the millisecond time scale, is overcome by calculating relative free energies using ball‐and stick local elevation umbrella sampling (B&S‐LEUS) to enhance the statistics on the relevant states and to promote interconversion transitions. Associated unbiased MD simulations also evidence for the first time a complete Vase ‐to‐Kite transition, as well as transitions between degenerate Kite 1 and Kite 2 forms and solvent‐exchange events. The calculated Vase ‐to‐Kite free‐energy changes ΔG are in qualitative agreement with the experimental magnitudes and trends. The level of quantitative agreement is, however, limited by the force‐field accuracy and, in particular, by the approximate treatment of intramolecular interactions at the classical level. The results are in line with a less stable Vase state for the dinitrobenzene compared to the quinoxaline compound, and a negative entropy change ΔS for the Vase ‐to‐Kite transition of the latter compound. Relative free energies calculated for intermediates also suggest that the Vase ‐Kite transition does not follow a concerted mechanism, but an asynchronous one with sequential opening of the flaps. In particular, the conformation involving two adjacent flaps open in a parallel direction (cis‐p) represents a likely intermediate, which has not been observed experimentally to date. 相似文献
3.
Yin Li Zsolt Csók László Kollár Koichi Iwata Erzsébet Szász 《Supramolecular chemistry》2013,25(6):374-378
2-Methylresorcinarene and its methylene-bridged cavitand derivative as host compounds were investigated in selective complexation of alkali metal ions as guests in methanol media by photoluminescence measurements. These host molecules possess either flexible (2-methylresorcinarene) or rigid (cavitand) molecular skeleton. The Benesi–Hildebrand method and the van't Hoff theory have been applied to determine the stability constants and the thermodynamic parameters, respectively. Considerable interactions between 2-methylresorcinarene and Li+ or Na+ ions have been observed while the rigid cavitand derivative can interact only with K+ or Cs+ ions. Neither the complexes of 2-methylresorcinarene with K+ or Cs+ nor those of the cavitand derivative with Li+ or Na+ ions are stable at room temperature in methanol media. Quantum-chemical investigations justified that only solvated Li+ and Na+ ions can form stable complexes with 2-methylresorcinarene while unsolvated K+ and Cs+ ions form stable complexes with the methylene-bridged cavitand. These results highlight that the stability of the guest solvation shell and its size could play a key role in the selectivity behaviour of host molecules. 相似文献
4.
Moonsuk Kang Sook Kyung Kim Bong-Gu Kang Kap Duk Lee Juyoung Yoon 《Journal of inclusion phenomena and macrocyclic chemistry》2003,46(3-4):155-159
A series of new cavitands containing four esters, nitriles, 2-pyridyl, or 3-pyridyl groups were synthesized fromtetrahydroxycavitand. Their binding properties towards various metal ions are investigated. 相似文献
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Reaction of the tripodal trilithium triamide [MeSi{SiMe2N(Li)(p‐Tol)}3(thf)2] ( 1 ) with SbCl3 in toluene gave the corresponding triaminostibine [MeSi{SiMe2N(p‐Tol)}3Sb] ( 2 ) in good yield. Its [2,2,2]bicyclooctane‐related cage structure, comprising the trisilylsilane unit and the triamidostibine fragment, was established by a single crystal X‐ray structure analysis: Space group P1, Z = 2, lattice dimensions at 293 K: a = 8.645(4), b = 10.029(5), c = 19.678(9) Å, α = 98.50(3)°, β = 97.46(3)°, γ = 94.80(3)°, R = 0.0216. 相似文献
6.
Brigitte BibalJean-Paul Declercq Jean-Pierre Dutasta Bernard TinantAnne-Gaëlle Valade 《Tetrahedron》2003,59(31):5849-5854
The iiii stereoisomer of the tetrathiophosphonate-calix[4]resorcinarene host 1 exhibited excellent extraction properties towards soft metal ions, with a better affinity for Ag+ (91%), than for Tl+ (38%) and Hg2+ (16%). The extraction of other picrate salts (Cu2+, Ni2+, Co2+, Zn2+, Cd2+, Pb2+) was not detected. The stoichiometry and the structure of the Hg2+, Tl+ and Ag+ complexes were studied by NMR in solution and gave respectively 1:1, 1:1 and 1:2 host-guest complexes. The formation of the self-assembled 12·(AgPic)4 complex was independent on the anion and only observed with silver(I) ion. 相似文献
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Kyungsoo Paek Linda M. Gutierrez Tunstad Emily F. Maverick Carolyn B. Knobler Donald J. Cram 《Journal of inclusion phenomena and macrocyclic chemistry》2003,45(3-4):203-209
A foot-to-foot or `back-to-back' connected biscavitand is prepared directly from a hexadecol resorcinarene precursor. The axial orientation of the biphenyl linker and hence the crown conformation of the hexadecol was established by an X-ray crystal study of the biscavitand. Each cavitand bowl is filled in the crystal by an alkyl `foot' from the next molecule, a self-inclusion which results in polymeric host–guest chains. The new biscavitand differs from previously prepared Z and C isomers of a bowl-to-bowl or `front-to-front' connected host, which crystallize as chains of carcerand-like, solvent-filled cages or as distinct molecules of hemicarceplex, respectively. 相似文献
9.
ChaoGuoYAN YunGE 《中国化学快报》2004,15(9):1019-1021
Three different synthetic routes were developed to introduce carbamoyloxy functional groups at the upper periphery of two calix[4]resorcinarenes. By treating activated esters 2a-b with excess corresponding amine such as 3-(dimethylamino)propylamine 3, ct-phenethylamine 4 and triethylenetetramine 5, six amide derivatives 6a-8b were obtained in high yield (Route 1). The pyridine-linked amide derivatives 9a-b were prepared by using acid chloride intermediate (Route 2).The amide derivatives 10a-b were obtained in moderate yields by direct alkylation of phenolic hydroxyl groups of la-b with N,N-dipropylchloroacetoamide in the presence of K2CO3/KI in acetone (Route 3). 相似文献
10.
基于大环自组装和多卤阴离子合成了有机-无机杂化超分子化合物,[(1,4-PMNH3)·(18-crown-6)]·[(H3O)·(18-crown-6)]2·[(H2O)·(18-crown-6)]·(18-crown-6)·(Bi2Cl9)(1)。化合物属正交晶系,Pca21空间群,a=2.483 0(3)nm,b=1.161 8(3)nm,c=3.316 1(2)nm,V=9.566(2)nm3。并通过其红外光谱、粉末衍射、热重分析和单晶结构分析对化合物进行了充分表征。在转子定子型的超分子化合物1中,大环超分子阳离子和(Bi2Cl9)3-阴离子交错堆积形成包合物结构。并在室温下对其固体荧光性质进行测试表征。通过DSC对其热稳定性进行了详细分析。 相似文献
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为深入开展杯芳烃为骨架的超分子拓扑结构的组装和性能,开展了间苯二酚杯芳烃八取代吡啶酰胺的合成和分子结构的研究。 以四丙基、四己基和四庚基间苯二酚杯芳烃为原料,使用α-氯乙酸甲酯实现O-烃基化,后者在无溶剂条件下与2-氨甲基吡啶反应实现酰胺化,制备了烷基间苯二酚杯芳烃八[N-(2-吡啶甲基)乙酰胺]衍生物。 用X衍射方法测定了四丙基间苯二酚杯芳烃八乙酸甲酯、四丙基以及四己基间苯二酚杯芳烃八[N-(2-吡啶甲基)乙酰胺]的单晶分子结构。 在晶体中,间苯二酚杯芳烃都以全顺式构型存在,在成环的四个间苯二酚单元中,1,3-位的两个间苯二酚单元处于近直立构象,2,4-位的另两个间苯二酚单元处于近平伏构象,而4个烷基皆处于分子的下缘,8个乙酰胺支链伸向分子的外围。 相似文献
12.
基于大环自组装和多卤阴离子合成了有机-无机杂化超分子化合物,[(1,4-PMNH3)·(18-crown-6)]·[(H3O)·(18-crown-6)]2·[(H2O)·(18-crown-6)]·(18-crown-6)·(Bi2Cl9)(1)。化合物属正交晶系,Pca21空间群,a=2.4830(3)nm,b=1.1618(3)nm,c=3.3161(2)nm,V=9.566(2)nm3。并通过其红外光谱、粉末衍射、热重分析和单晶结构分析对化合物进行了充分表征。在转子定子型的超分子化合物1中,大环超分子阳离子和(Bi2Cl9)3-阴离子交错堆积形成包合物结构。并在室温下对其固体荧光性质进行测试表征。通过DSC对其热稳定性进行了详细分析。 相似文献
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在水热条件下合成了一种新的二帽二支撑的Keggin型钼钒多金属氧酸盐[Cu(2,2'-bpy)3]{[Cu(2,2'-bpy)2]2HPⅤMo 8 VI V 6 IV O42]}·2H2O(1,bpy=联吡啶),利用元素分析、红外光谱、X射线光电子能谱,粉末和X射线单晶衍射等分析技术对化合物的晶体结构进行了表征。 结果表明,该化合物属于单斜晶系,C2/c空间群,a=2.8734(3) nm,b=1.47333(12) nm,c=2.31023(16) nm,β=112.509(5)°,V=9.0351(12) nm3,Z=1,R1=0.0489,wR2=0.1286。 化合物的阴离子是二帽α-Keggin结构P/Mo/V多金属氧簇,通过簇阴离子两个钒帽上的端氧分别支撑两个铜过渡金属配合物,化合物簇阴离子,水分子和2,2'-联吡啶分子之间通过π-π和氢键作用形成了三维超分子结构。 相似文献
14.
A molecular bowl with barium ion covering one portal of decamethylcucurbit[5]uril as a ‘metal-ion-bottom’ has been synthesized. The structure of the molecular bowl has been confirmed by the single crystal X-ray diffraction determination. It belongs to orthorhombic with space group of
Pna21. The crystal unit cell parameters are: a=3.210 8(6) nm, b=1.474 2(3) nm, c=1.151 6(2) nm, and V=5.450 9(18)
nm3, Dc=1.677 Mg·m-3, Z=4, F(000)=2 832, R=0.055 1, wR=0.156 8. CCDC: 290552. 相似文献
15.
HAN Jun GE Yun YAN Chao-guo 《高等学校化学研究》2006,22(4):537-542
IntroductionOver the past two decades, dendrimers have at-tracted considerable attention because of their inherentnovel structural features and their potential applicationsin various scientific and industrial fields such as cataly-sis or newmaterials, and… 相似文献
16.
The synthesis and X-ray crystal structure of a new molecular clip 2 was reported. It (C24H24N4O2, Mr = 400.47) crystallizes in the space group C2/c with a = 15.587(2), b = 8.5805(12), c = 15.259(2) A, β = 102.448(3)°, V= 1992.9 (5)A63, Z = 4, Dc = 1.335 g/cm63,μ = 0.087 mm^-1 and F(000) = 848. It remains monomeric in the crystal and a tape-like structure is formed in the crystal structure of molecular clip. The most unusual structural feature of 2 is the boat conformation of its cyclohexyl ring imposed by the ring fusion at C(9)-C(9a). 相似文献
17.
以Mg(OH)2和NaAlO2为原料,采用新原料路线共沉淀法实现了柠檬酸根插层结构LDHs的超分子组装。用XRD、FT-IR、TG-DTA和元素分析等手段对样品进行分析表征。结果表明,新原料路线共沉淀法较常用的共沉淀法得到的柠檬酸根插层LDHs结晶度高、晶相单一,客体柠檬酸根在LDHs层间的排列高度有序。 相似文献
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以PEG-400为固液相转移催化剂,通过苯甲酰氯与硒氰酸钾反应合成了中间体苯甲酰基异硒氰酸酯,该中间体不需分离,直接与芳胺反应,得到N-苯甲酰基-N'-芳基硒脲(2a~2p),这些化合物用1HNMR,IR及元素分析进行了表征,并用X射线单晶衍射确定了化合物2k的单晶结构.晶体结构表明,该化合物通过分子间氢键组装成了沿a轴无限延伸的一维链状超分子结构.晶体属于单斜晶系,P2(1)/c空间群,晶胞参数:a=1.1073(1)nm,b=0.5745(1)nm,c=2.4356(5)nm,β=92.10(1)°,V=1.5483(4)nm3,Z=4,μ=2.428. 相似文献
20.
Yan XU Hai Xian WANG Yong FU Mao Ping SONG Yang Jie WU* Department of Chemistry Henan Key Laboratory of Applied Chemistry Henan Key Laboratory of Chemical Biology organic chemistry Zhengzhou University Zhengzhou 《中国化学快报》2005,16(7):883-885
Ferrocene and the derivatives play an important role in organometallic chemistry due to their potential novel functions and applications. Of particular interest is an electron-transfer system of ion center for molecular electronics1. Several efforts have been directed towards the design and synthesis of multi-electron redox mediators that could transfer several electrons simultaneously at the same potential2. It was reported that ferrocenylphenyl group was an excellent electron transfer mediat… 相似文献