排序方式: 共有21条查询结果,搜索用时 15 毫秒
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Dr. Tanya K. Ronson Chandan Giri Dr. N. Kodiah Beyeh Antti Minkkinen Filip Topić Dr. Julian J. Holstein Prof. Kari Rissanen Dr. Jonathan R. Nitschke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(10):3374-3382
Subtle differences in metal–ligand bond lengths between a series of [M4L6]4? tetrahedral cages, where M=FeII, CoII, or NiII, were observed to result in substantial differences in affinity for hydrophobic guests in water. Changing the metal ion from iron(II) to cobalt(II) or nickel(II) increases the size of the interior cavity of the cage and allows encapsulation of larger guest molecules. NMR spectroscopy was used to study the recognition properties of the iron(II) and cobalt(II) cages towards small hydrophobic guests in water, and single‐crystal X‐ray diffraction was used to study the solid‐state complexes of the iron(II) and nickel(II) cages. 相似文献
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N. Kodiah Beyeh 《Tetrahedron letters》2009,50(52):7369-7373
The direct reaction between 2-nitroresorcinol and acetaldehyde in alkaline medium yields tetranitro-C1-resorcin[4]arene in a moderate 8.2% overall yield which was characterized by single crystal X-ray crystallography, 1H NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS). In solution and in the solid state, the product adopts a unique, thermally stable and unprecedented rcct-boat conformation. 相似文献
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Dr. Ngong Kodiah Beyeh Dr. Fangfang Pan Acad. Prof. Kari Rissanen 《Angewandte Chemie (International ed. in English)》2015,54(25):7303-7307
Iodine (I2) acts as a bifunctional halogen‐bond donor connecting two macrocyclic molecules of the bowl‐shaped halogen‐bond acceptor, N‐cyclohexyl ammonium resorcinarene chloride 1 , to form the dimeric capsule [(1,4‐dioxane)3@ 1 2(I2)2]. The dimeric capsule is constructed solely through halogen bonds and has a single cavity (V=511 Å3) large enough to encapsulate three 1,4‐dioxane guest molecules. 相似文献
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Dr. N. Kodiah Beyeh Dr. Fangfang Pan Dr. Sandip Bhowmik Toni Mäkelä Prof. Robin H. A. Ras Acad. Prof. Kari Rissanen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(4):1355-1361
N‐Alkyl ammonium resorcinarene salts (NARYs, Y=triflate, picrate, nitrate, trifluoroacetates and NARBr) as tetravalent receptors, are shown to have a strong affinity for chlorides. The high affinity for chlorides was confirmed from a multitude of exchange experiments in solution (NMR and UV/Vis), gas phase (mass spectrometry), and solid‐state (X‐ray crystallography). A new tetra‐iodide resorcinarene salt (NARI) was isolated and fully characterized from exchange experiments in the solid‐state. Competition experiments with a known monovalent bis‐urea receptor ( 5 ) with strong affinity for chloride, reveals these receptors to have a much higher affinity for the first two chlorides, a similar affinity as 5 for the third chloride, and lower affinity for the fourth chloride. The receptors affinity toward chloride follows the trend K1?K2?K3≈ 5 >K4, with Ka=5011 m ?1 for 5 in 9:1 CDCl3/[D6]DMSO. 相似文献
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Kalenius E Beyeh NK Jänis J Rissanen K 《Chemical communications (Cambridge, England)》2011,47(9):2649-2651
Pyrogallarene shows concentration-dependent instability in dilute solutions resulting in elimination of two ketene molecules and formation of pyrogallarene lactones. This unexpected phenomenon, which is not observed with resorcinarenes, highlights the significance of the four hydroxyl groups at 2-position for the molecular characteristics of pyrogallarenes. 相似文献
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Ngong K. Beyeh Domonkos Fehér Minna Luostarinen Christoph A. Schalley Kari Rissanen 《Journal of inclusion phenomena and macrocyclic chemistry》2006,56(3-4):381-394
The syntheses and characterization of new chiral tetrabenzoxazine and tetrakis-(dialkylaminomethyl) resorcinarenes can be
achieved through the reaction of resorcinarene with chiral amines and formaldehyde. In order to examine their host–guest chemistry,
chiral quaternary ammonium guests were synthesized by methylation of different amines and amino acid methyl esters through
a reductive methylation followed by addition of methyl iodide. Subsequent anion exchange of the iodide against tetraphenylborate
helps to improve solubility of the salts in organic solvents. After characterization in solution, mass spectrometry is used
to examine the resorcinarenes’ chemistry in the gas phase. Interesting implications of the fragmentation behavior for their
solution phase chemistry arise, for which a first example is presented. Ammonium ion binding is indicated by mass spectrometry.
Nevertheless, chiral recognition between the chiral hosts and pseudoracemic 1:1 mixtures of appropriately deuterium-labeled
chiral guest cations is however not observed. 相似文献
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Beyeh NK Weimann DP Kaufmann L Schalley CA Rissanen K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(18):5552-5557
The non-covalent interactions of different upper-rim-substituted C(2)-resorcinarenes with tetramethylammonium salts were analyzed in the gas phase in an Electrospray Ionization Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometer and by (1)H NMR titrations. The order of binding strengths of the hosts towards the tetramethylammonium cation in the gas phase reflects the electronic nature of the substituents on the upper rim of the resorcinarene. In solution, however, a different trend with particularly high binding constants for halogenated resorcinarenes has been observed. This trend can be explained by a synergetic effect originating from the interaction of the halogenated resorcinarenes with the counter anions through hydrogen bonding. This study highlights the importance of weak interactions in recognition processes and points out the benefits of comparing the gas-phase data with results obtained from solution experiments. 相似文献
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Ahmed Shaukat Dr. Eduardo Anaya-Plaza Prof. Ngong Kodiah Beyeh Prof. Mauri A. Kostiainen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(11):e202104341
Supramolecular self-assembly of biomolecules provides a powerful bottom-up strategy to build functional nanostructures and materials. Among the different biomacromolecules, protein cages offer various advantages including uniform size, versatility, multi-modularity, and high stability. Additionally, protein cage crystals present confined microenvironments with well-defined dimensions. On the other hand, molecular hosts, such as cyclophanes, possess a defined cavity size and selective recognition of guest molecules. However, the successful combination of macrocycles and protein cages to achieve functional co-crystals has remained limited. In this study, we demonstrate electrostatic binding between cationic pillar[5]arenes and (apo)ferritin cages that results in porous and crystalline frameworks. The electrostatically assembled crystals present a face-centered cubic (FCC) lattice and have been characterized by means of small-angle X-ray scattering and cryo-TEM. These hierarchical structures result in a multiadsorbent framework capable of hosting both organic and inorganic pollutants, such as dyes and toxic metals, with potential application in water-remediation technologies. 相似文献