Thematische Bibliographien / Host-Guest inclusion complex

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  1. Zeitschriftenartikel
  2. Dissertationen
  3. Buchteile
  4. Konferenzberichte

Auswahl der wissenschaftlichen Literatur zum Thema „Host-Guest inclusion complex“

Autor: Grafiati
Veröffentlicht am 18. Mai 2024

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Zeitschriftenartikel zum Thema "Host-Guest inclusion complex"

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Tanaka, Koichi, Naoki Daikawa und Shigeru Ohba. „Novel Bisurea Host Compounds“. Journal of Chemical Research 2002, Nr. 11 (November 2002): 579–81. http://dx.doi.org/10.3184/030823402103170853.

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New host molecules, 4,4′-bis(dimethylamino-urea)diphenylmethane (1) and its derivatives (2 and 3), are reported. These hosts are shown to give inclusion complex crystals with a wide variety of organic guest molecules with high selectivity. The crystal structure of 1:2 inclusion complex of 1 with THF has been determined from X-ray crystal structure analysis. The cyclic N–H...O intermolecular hydrogen bonds between host molecules were found to form columns for accommodation of the guest molecules.
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Li, Chun-Rong, Hua-Ming Feng, Jin-Yi Zhao, Zhu Li, Bing Bian, Tie-Hong Meng, Xian-Yun Hu, Heng Wang und Xin Xiao. „Supramolecular Interaction Between Cucurbit[8]uril and the Quinolone Antibiotic Ofloxacin“. Australian Journal of Chemistry 72, Nr. 12 (2019): 983. http://dx.doi.org/10.1071/ch19341.

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The host–guest inclusion complex of cucurbit[8]uril (Q[8]) and ofloxacin (OFLX) has been prepared and characterised by means of 1H NMR spectroscopy, MALDI-TOF mass spectrometry, isothermal titration calorimetry (ITC), fluorescence spectroscopy, and UV-vis absorption spectroscopy. The findings demonstrated that a host–guest inclusion complex could be formed through an encapsulation of the methylmorpholine and piperazine rings in OFLX. ITC results indicated that the formation of this inclusion complex (1:1 molar ratio) was primarily dependent on enthalpy and entropy changes. In addition, the release of OFLX from the inclusion complex was increased under acidic conditions.
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Wagner, Brian D., Shannon J. Fitzpatrick, Monica A. Gill, Andrew I. MacRae und Natasa Stojanovic. „A fluorescent host-guest complex of cucurbituril in solution: a molecular Jack O'Lantern“. Canadian Journal of Chemistry 79, Nr. 7 (01.07.2001): 1101–4. http://dx.doi.org/10.1139/v01-094.

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Fluorescence enhancement of a probe molecule in solution by the container molecule cucurbituril (CB) is reported for the first time. The fluorescence of the probe 2-anilinonaphthalene-6-sulfonate (2,6-ANS) in aqueous Na2SO4 solution is found to increase by a maximum factor of 5.0 upon addition of cucurbituril. This fluorescence enhancement is the result of the formation of a host–guest inclusion complex, in which the guest 2,6-ANS is incorporated inside the cavity of the host, cucurbituril. Measurement of the enhancement as a function of cucurbituril concentration yielded a value of the equilibrium constant (K) of 52 ± 10 M–1. It is proposed that the mode of inclusion involves the phenyl group of the 2,6-ANS, because of the relatively small size of the cucurbituril cavity. It is further proposed that the observed enhancement is a result of loss of rotational mobility of the phenyl ring relative to the naphthyl fluorophore of 2,6-ANS upon inclusion of the phenyl ring. Since the name cucurbituril is derived from the Latin word for "pumpkin," this fluorescent host-guest complex is referred to as a "molecular Jack O'Lantern," with the 2,6-ANS serving as the candle.Key words: host–guest chemistry, fluorescence, cucurbituril, inclusion compounds.
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Tahir, M. Nazir, Yihong Cao, Abdelkrim Azzouz und René Roy. „Host-guest chemistry of the sulfasalazine-β-cyclodextrin inclusion complex“. Tetrahedron 85 (April 2021): 132052. http://dx.doi.org/10.1016/j.tet.2021.132052.

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D’Aria, Federica, Carla Serri, Marcella Niccoli, Laura Mayol, Vincenzo Quagliariello, Rosario Vincenzo Iaffaioli, Marco Biondi und Concetta Giancola. „Host–guest inclusion complex of quercetin and hydroxypropyl-β-cyclodextrin“. Journal of Thermal Analysis and Calorimetry 130, Nr. 1 (16.02.2017): 451–56. http://dx.doi.org/10.1007/s10973-017-6135-5.

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Aramoto, Hikaru, Motofumi Osaki, Subaru Konishi, Chiharu Ueda, Yuichiro Kobayashi, Yoshinori Takashima, Akira Harada und Hiroyasu Yamaguchi. „Redox-responsive supramolecular polymeric networks having double-threaded inclusion complexes“. Chemical Science 11, Nr. 17 (2020): 4322–31. http://dx.doi.org/10.1039/c9sc05589d.

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Alrawashdeh, Lubna, Khaleel I. Assaf, Walhan Alshaer, Fadwa Odeh und Suhair A. Bani-Atta. „Preparation, characterization, and biological activity study of thymoquinone-cucurbit[7]uril inclusion complex“. RSC Advances 12, Nr. 4 (2022): 1982–88. http://dx.doi.org/10.1039/d1ra08460g.

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Wilson, Lee D., und Ronald E. Verrall. „A 1H NMR study of cyclodextrin - hydrocarbon surfactant inclusion complexes in aqueous solutions“. Canadian Journal of Chemistry 76, Nr. 1 (01.01.1998): 25–34. http://dx.doi.org/10.1139/v97-208.

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A 1H NMR chemical shift ( delta ) study of a homologous series of hydrocarbon (hc) (CxH2x + 1CO2Na, x = 5, 7, 9, 11, 13) surfactants (S) has been carried out in water and in binary solvent (D2O + cyclodextrin (CD)) systems at 22°C. Complementary 1H NMR chemical shift ( delta ) data of the cyclodextrins in binary (D2O + S) systems containing hc surfactants have also been obtained. Complex induced shift (CIS) values for selected host or guest protons were found to increase as the alkyl chain (Cx) length of the surfactant increased. The CIS values are found to depend on the following factors: (i) the magnitude of the binding constant (Ki, i = 1:1, 2:1), (ii) the chain length of the surfactant, (iii) the mole ratio of the host to guest species, (iv) the host-guest stoichiometry, and (v) the host-guest inclusion geometry. The CIS values of the CD-S systems have been analyzed using equilibrium models in which 1:1 complexes, 1:1 plus 2:1 complexes, and uncomplexed species are present. Differences in the binding affinity, stoichiometry, and inclusion geometry of the complexes formed between a given hc surfactant and the various cyclodextrins were observed.Key words: cyclodextrin, surfactant, NMR, chemical shift, complex, binding constant.
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Zhou, Jiong, Bin Hua, Li Shao, Hao Feng und Guocan Yu. „Host–guest interaction enhanced aggregation-induced emission and its application in cell imaging“. Chemical Communications 52, Nr. 33 (2016): 5749–52. http://dx.doi.org/10.1039/c6cc01860b.

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A host–guest inclusion complex based on a monofunctionalized pillar[5]arene and a tetraphenylethene derivative was prepared, resulting in an enhanced emission from the tetraphenylethene-based guest, which was applied in cell imaging.
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Rahaman, Habibur, Niloy Roy, Aditi Roy, Samapika Ray und Mahendra Nath Roy. „Exploring Existence of Host-Guest Inclusion Complex of β-Cyclodextrin of a Biologically Active Compound with the Manifestation of Diverse Interactions“. Emerging Science Journal 2, Nr. 5 (04.11.2018): 251. http://dx.doi.org/10.28991/esj-2018-01149.

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The host–guest interaction of p-nitro benzaldehyde as guest β-Cyclodextrins have been investigated which have significant applications in the field of medicine such as controlled drug delivery. The 1H NMR study confirms the formation of inclusion complex while surface tension and conductivity studies support the formation inclusion complex with 1:1 stoichiometry. The stoichiometry of the inclusion complex was also supported with Job’s plot method by UV-Visible spectroscopy. FT-IR spectra and SEM study also support the inclusion process. Association constants of the inclusion complexes have been calculated using the Benesi–Hildebrand method, while the thermodynamic parameters have been estimated with the help of van’t Hoff equation.
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Dissertationen zum Thema "Host-Guest inclusion complex"

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Roy, Aditi. „Study to explore molecular inclusion complexes of cyclic hosts with vital guests in various environments“. Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2633.

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Daver, Henrik. „Quantum Chemical Modeling of Phosphoesterase Mimics and Chemistry in Confined Spaces“. Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-148259.

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In this thesis, density functional theory is employed in the study of two kinds of systems that can be considered to be biomimetic in their own ways. First, three binuclear metal complexes, synthesized by the group of Prof. Ebbe Nordlander, have been investigated. The complexes are designed to resemble the active sites of phosphatase enzymes and have been examined in complexes where either two Zn(II) ions or one Fe(III) and one Mn(II) ion are bound. These dinuclear compounds were studied as catalysts for the hydrolysis of bis(2,4-dinitrophenyl) phosphate and the transesterification of 2-hydroxypropyl p-nitrophenyl phosphate, which are model systems for the same reactions occurring in DNA or RNA. It was found that the two reactions take place in similar ways: a hydroxide ion that is terminally bound to one of the metal centers acts either as a nucleophile in the hydrolysis reaction or as a base in the transesterification. The leaving groups depart in an effectively concerted manner, and the formed catalyst-product complexes are predicted to be the resting states of the catalytic cycles. The rate-determining free energy barriers are identified from the catalyst-product complex in one catalytic cycle to the transition state of nucleophilic attack in the next. Another type of biomimetic modeling is made with an aim of imitating the conceptual features of selective binding of guests and screening them from solute-solvent interactions. Such features are found in so-called nanocontainers, and this thesis is concerned with studies of two capsules synthesized by the group of Prof. Julius Rebek, Jr. First, the cycloaddition of phenyl acetylene and phenyl azide has experimentally been observed to be accelerated in the presence of a capsule. Computational studies were herein performed on this system, and a previously unrecognized structure of the capsule is discovered. Two main factors are then identified as sources of the rate acceleration compared to the uncatalyzed reaction, namely the reduction of the entropic component and the selective destabilization of the reactant supercomplex over the transition state. In the second capsule study, the alkane binding trends of a water-soluble cavitand was studied. It is found that implicit solvation models fail severely in reproducing the experimental equilibrium observed between binding of n-decane by the cavitand monomer and encapsulation in the capsule dimer. A mixed explicit/implicit solvation protocol is developed to better quantify the effect of hydrating the cavitand, and a simple correction to the hydration free energy of a single water molecule is proposed to remedy this. The resulting scheme is used to predict new hydration free energies of the cavitand complexes, resulting in significant improvement vis-à-vis experiments. The computational results presented in this thesis show the usefulness of the quantum chemical calculations to develop understanding of experimental trends observed for substrate binding and catalysis. In particular, the methodology is shown to be versatile enough such that experimental observations can be reproduced for such diverse systems as studied herein.

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 5: Manuscript.

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Bezuidenhout, Charl Xavier. „Polar ordering of guest molecules in host-guest inclusion complexes“. Thesis, Stellenbosch : Stellenbosch University, 2011. http://hdl.handle.net/10019.1/18107.

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Thesis (MSc)--Stellenbosch University, 2011.
ENGLISH ABSTRACT: 2,7-dimethylocta-3,5-diyne-2,7-diol forms inclusion complexes with various guests molecules, where the guest molecules are polar-ordered. A Cambridge Structural Database (CSD) search revealed ten inclusion complexes where the guest molecules were polar-ordered. Using Density Functional Theory (DFT) computational methods (in the absence of the host), we evaluated the intra-channel and lateral guest-guest interactions between the guest molecules. Two polar-ordered inclusion complexes ((1,4,7-cyclohexane-1,2,4,5,7,8-hexaoxonane)·CHCl3 and (2,4,6-(endolongifolyl)-1,3,5-trioxane)·CDCl3) were singled out in the CSD search for further studies along with 2,7-dimethylocta-3,5-diyne-2,7-diol. Synthesis of any 1,2,4,5,7,8-hexaoxonane and 1,3,5-trioxane derivatives was attempted to establish whether the polar-ordering ability extends into the family of compounds. We managed to produce three new polar-ordered inclusion complexes with 2,7-dimethylocta-3,5-diyne-2,7-diol (ClC(CH3)3, BrC(CH3)3 and IC(CH3)3), thus extending the series to six guest polar-ordered systems. We were only able to synthesise 1,4,7-cyclohexane-1,2,4,5,7,8-hexaoxonane and produce the CHCl3 inclusion complex and one new polar-ordered inclusion complex (CHBr3). Three 1,3,5-trioxanes was synthesised (the cyclohexyl, cyclohex-3-en-1-yl and cyclopentyl derivatives), which did not include any solvents. However, these 1,3,5-trioxanes also form polar-ordered crystals. These compounds and inclusion complexes were analysed by means of single crystal X-ray diffraction to determine their crystal structures. All the crystal structures could be solved and refined to adequate accuracy (except for 2,4,6-tri(cyclopentyl)-1,3,5-trioxane) with no disorder of the guest molecules (where applicable) and their polar-ordering property investigated. Due to their vast molecular differences, these compounds were studied separately by means of visual crystal structure analysis and computational modelling techniques (Density functional theory, molecular mechanics, molecular dynamics and molecular quench dynamics).
AFRIKAANSE OPSOMMING: 2,7-dimetielokta-3,5-diyn-2,7-diol vorm insluitingskomplekse met verskeie molekules as gaste, waar die gas-molekules polêr georden is. 'n Cambridge Struktuur Databasis (CSD) soektog lewer tien insluitings komplekse waarvan die gas-molekules polêr georden is. Deur gebruik te maak van Digtheidsfunksionele teorie (DFT) berekeninge (in die afwesigheid van die gasheer) het ons die inter-kanaal en wedersydse gas-gas interaksies tussen die gas molekules geëvalueer. Twee polêr geordende insluitingskomplekse ((1,4,7-sikloheksaan-1,2,4,5,7,8-heksaoksonaan)·CHCl3 en (2,4,6-(endolongifolyl)-1,3,5-trioksaan)·CDCl3) is uitgesonder uit die CSD soektog vir verdere studies saam met 2,7-dimetielokta-3,5-diyn-2,7-diol. Aanslag was gemaak om enige 1,2,4,5,7,8-heksaoksonaan en 1,3,5-trioksaan derivate te sintetiseer en vas te stel of die polêre ordensvermoë oor die familie van verbindings strek. Ons het daarin geslaag om drie nuwe polêr geordende insluitingskomplekse op te lewer met 2,7-dimetielokta-3,5-diyn-2,7-diol (Cl(CH3)3, BrC(CH3)3 en I(CH3)3), en sodoende die reeks uitgebrei na ses gaste wat polêr geordende insluitingskomplekse vorm. Net 1,4,7-sikloheksaan-1,2,4,5,7,8-heksaoksonaan kon gesintetiseer word en dit lewer twee polêr geordende insluitingskomplekse (CHCl3 en CHBr3 (nuut)). Drie 1,3,5-trioksane is gesintetiseer (die sikloheksiel, sikloheks-3-een-1-iel en siklopentiel derivate) en het nie enige oplosmiddels (gaste) ingesluit nie. Nietemin vorm hiedie 1,3,5-trioksane ook polêr geordende kristalle. Hierdie verbindings en insluitingskomplekse is geanaliseer deur middel van enkelkristal X-straal diffraksie om hul kristalstrukture te bepaal. Alle kristalstrukture was opgelos en verwerk tot voldoende akkuraatheid (behalwe vir 2,4,6-tri(siklopentiel)-1,3,5-trioxane) met geen wanorde in die gas molekuul posisies nie (waar van toepassing) en hul polêre ordensvermoë is ondersoek. As gevolg van groot verskille in hul molekulêre strukture, is hierdie verbindings afsonderlik bestudeer deur middel van molekulêre modellerings metodes (Digtheidsfunksionele teorie, molekulêre meganika, molekulêre dinamika en molekulêre stakings dinamika).
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Kundu, Mitali. „Exploration of inclusion complexes between host and guest molecules and solvation effect of some vital molecules in various environments“. Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2689.

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O'Brien, Mark. „Spectroscopic Studies of Inclusion Host-Guest Complexes Between Cyclophane Corrals and Polcyclic Aromatic Hydrocarbons“. TopSCHOLAR®, 2005. http://digitalcommons.wku.edu/theses/470.

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Cyclophanes are macromolecules that are known to effectively bind with molecules to form host-guest complexes. Several cyclophane molecules, referred to as corrals (1-6) by their founders, have been synthesized. The characterization of these compounds and their complexes has been investigated using combined spectroscopic and theoretical methods. Hostguest interactions of cyclophane-anthracene (C-A), cyclophane-9-fluorenone (C-F) and cyclophane-pyrene (C-P) complex systems in dichloromethane are presented in this thesis. The stability constants, log Ka, for the C-A, C-F and C-P complexes are determined using absorption and fluorescence spectroscopy. Heats of formation of corral 2 complexes were determined by measuring the complex association constants at 25, 29 and 32 °C. Results reveal that binding of the non-polar guests by the cyclophane molecules are thermodynamically favored over binding with polar guest. Computational studies indicate difference in energy due to solvent effect of the complexes in the condensed phase. Excited state lifetimes of these systems are also determined, and they support fluorescence as a path of relaxing back to the ground state.
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Mondal, Jaygopal. „Solvation consequences of different aqueous media on some biologically active compounds: a physico-chemical study“. Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4751.

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Barman, Siti. „Investigation on solvation behaviour and host guest inclusion complexes of some significant molecules with diverse cyclic compounds“. Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2588.

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Groom, Jazerie J. „Evaluation of Apparent Formation Constants of Host-Guest Inclusion Complexes of Solutes with Soluble Calixarenes Using High Performance Liquid Chromatography“. Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1389273191.

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Saha, Binoy Chandra. „Host guest inclusion complexes and thermodynamic properties of some imperative molecules with the manifestation of diverse interections by physiochemical investigation“. Thesis, University of North Bengal, 2020. http://ir.nbu.ac.in/handle/123456789/3966.

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Rahaman, Habibur. „Diverse Interactions of Some Significant Compounds Prevailing in Different Solvent Systems with the Manifestation of Solvation Consequence by Physicochemical Investigations“. Thesis, University of North Bengal, 2019. http://ir.nbu.ac.in/handle/123456789/2814.

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Buchteile zum Thema "Host-Guest inclusion complex"

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Wagner, Brian D. „Host–Guest Inclusion Complexes“. In Supramolecular Chemistry in Corrosion and Biofouling Protection, 17–40. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003169130-3.

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Cheetham, A. K., und B. K. Peterson. „Computer Simulations of Host-Guest Complexes“. In Inclusion Phenomena and Molecular Recognition, 277–87. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0603-0_29.

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Toda, Fumio. „Reaction control of guest compounds in host-guest inclusion complexes“. In Topics in Current Chemistry, 211–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/3-540-19338-3_5.

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Wagner, Brian D. „Fluorescence Studies of the Hydrogen Bonding of Excited-State Molecules within Supramolecular Host-Guest Inclusion Complexes“. In Hydrogen Bonding and Transfer in the Excited State, 175–91. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470669143.ch8.

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González-Gaitano, G., T. Sanz, R. Gabarró, J. A. Rodríguez-Cheda, M. C. Sáez und G. Tardajos. „Molar Partial Properties in Host-Guest Systems: Application to the Inclusion Complexes between β- Cyclodextrin and Sodium Alkanoates“. In Proceedings of the Ninth International Symposium on Cyclodextrins, 667–70. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4681-4_158.

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Vitale, Rosa Maria, und Pietro Amodeo. „Self-Inclusion Complexes of Monofunctionalized Beta-Cyclodextrins as Host–Guest Interaction Model Systems and Simple and Sensitive Testbeds for Implicit Solvation Methods“. In Computational Electrostatics for Biological Applications, 271–96. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-12211-3_14.

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Ebmeyer, Frank, und Fritz Vogtle. „New hosts for the molecular recognition and encapsulation of guest compounds“. In Inclusion Compounds, 263–82. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552925.003.0006.

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Abstract The past decade has witnessed an upsurge of interest in molecular recognition processes. Whereas the syntheses of new host structures initially stood to the fore, more recent studies have concentrated on the selectivity of supramolecular structures, on hydrophobic interactions, base pairing due to hydrogen bridges, hydrogen bridging in the interior of molecular niches, complexation of anions, and highly selective and extremely efficient cation complexation. Whilst simple cation complexation by use of crown compounds, cryptands, and podands is understood quite well at the present time, and is used synthetically, more complex synthetic host structures often exhibit surprising properties. Triply bridged macrobicyclic host structures, constructed according to a modular building concept, have aroused special interest. They allow the construction of tailor-shaped host cavities, which encapsulate the guest almost completely. If intraannular donor functions are present, varying receptor capabilities are obtained. Yet, unfunctionalized molecular niches allowing hydrophobic interactions have also attracted attention.
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Harata, Kazuaki. „Recent advances in the X-ray analysis of cyclodextrin complexes“. In Inclusion Compounds, 311–44. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552932.003.0009.

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Abstract Cyclodextrins are cyclic oligosaccharides consisting of six or more a-1,4-linked o-glucose units. These bucket-shaped macrocyclic molecules have a cylindrical cavity with a diameter larger than 5 A and a depth of7-8 A. The inside wall of the macrocycle is comprised of many methylene and methine groups, whereas at both ends of the cavity hydroxy groups are found in a circular arrangement. Therefore, the cyclodextrin cavity exhibits hydrophobic character and favourably accommodates the hydrophobic portion of the guest. Cyclodextrins form inclusion complexes rather nonspecifically with a wide variety of guests of suitable size and shape. Because of the rigid structure of cyclodextrin molecules, the size and shape of the interior cavity are strictly confined by the number of constituent glucose units and complex formation is highly stereoselective, that is, guest molecules or groups should fit into the host cavity, even if only partially.
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Iwamoto, Toschitake. „Inclusion compounds of multi-dimensional cyanometal complex hosts“. In Inclusion Compounds, 177–212. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552932.003.0006.

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Abstract The cyanide group, CN-, is able to build up one- (1D), two- (2D), or three-dimensional (3D) frameworks by alternately linking one metal atom M to another metal atom M’. The M’—CN—M linkage is usually colinear; in some cases the M'—C—N or M—N—C bond, or both, bends to a certain extent. The deviation from colinearity is, however, not appreciable in comparison with the case of another ambidentate pseudohalogen group SCN-: the M’—SCN—M linkage is generally bent at the sulphur atom with an approximately tetrahedral angle. The sp hybridization character of the —C=N triple bond may contribute to the colinearity of the M’—CN—M linkage. One can easily depict the structure of a multi-dimensional framework comprised of the linear M'—CN—M linkages with the Mand M’ metal cations taking particular configurations of the respective coordination spheres: a ball- and-stick model is effective to depict the multi-dimensional host structure which can accommodate guest species.
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Andreetti, Giovanni D., Franco Ugozzoli, Rocco Ungaro, und Andrea Pochini. „Inclusion of ions and neutral molecules in calixarenes“. In Inclusion Compounds, 64–125. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552925.003.0003.

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Abstract The design and synthesis of molecular systems which perform chemical, physical, and biomimetic transformations with high efficiency and selectivity, and the understanding of the factors which determine the selective molecular recognition are two of the major aims of host-guest or supramolecular chemistry. In this novel multidisciplinary research area there is a continuous need for new building blocks, shaping units, or substructures which can be easily functionalized to build up more complex structures able to perform a particular transformation. Since the pioneering work of Gutsche and Muthukrishnan, Gutsche et al., and ourselves, which was mainly devoted to establishing the structures of the cyclic products formed by the base-catalyzed condensation of phenols and formaldehyde, the calixarenes (1)-(4) (see the preceeding chapter by Gutsche) have become rather popular among the chemical community.
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Konferenzberichte zum Thema "Host-Guest inclusion complex"

1

Hu, Shenshui, Cuiling Xu, Lingzi Meng, Yongbin He und Dafu Cui. „Electrochemical oxygen sensor based on host-guest inclusion complex of calixarene and methyl viologen“. In International Conference on Sensors and Control Techniques (ICSC2000), herausgegeben von Desheng Jiang und Anbo Wang. SPIE, 2000. http://dx.doi.org/10.1117/12.385597.

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2

Vázquez Tato, José, Víctor Soto Tellini, Aida Ramos, Juan Trillo Novo, Francisco Meijide und Jorge Carrazana G. „Can Guest Hydrophobicity Guide the Entrance into the Host in the Formation of an Inclusion Complex?“ In The 8th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01996.

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3

Kaneko, Takuma, Hirokazu Takahashi, Kenryo Ohminami, Takehisa Konishi, Masaki Ueda, Shin-ichi Nagamatsu und Takashi Fujikawa. „Host-Guest Interaction in α-Cyclodextrin Inclusion Complexes“. In X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644519.

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