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Artykuły w czasopismach na temat "Host-Guest moleculars"
Malinska, Maura. "Insights into molecular recognition from the crystal structures of p-tert-butylcalix[6]arene complexed with different solvents". IUCrJ 9, nr 1 (16.11.2021): 55–64. http://dx.doi.org/10.1107/s2052252521010678.
Pełny tekst źródłaChen, Kaifei, Seyed Hesam Mousavi, Ranjeet Singh, Randall Q. Snurr, Gang Li i Paul A. Webley. "Gating effect for gas adsorption in microporous materials—mechanisms and applications". Chemical Society Reviews 51, nr 3 (2022): 1139–66. http://dx.doi.org/10.1039/d1cs00822f.
Pełny tekst źródłaLebedinskiy, Konstantin, Ivan Barvík, Zdeněk Tošner, Ivana Císařová, Jindřich Jindřich i Radim Hrdina. "Spatial arrangements of cyclodextrin host–guest complexes in solution studied by 13C NMR and molecular modelling". Beilstein Journal of Organic Chemistry 20 (20.02.2024): 331–35. http://dx.doi.org/10.3762/bjoc.20.33.
Pełny tekst źródłaElemans, Johannes A. A. W., Roeland J. M. Nolte i Alan E. Rowan. "Hierarchical self-assembly of a host-guest porphyrin array". Journal of Porphyrins and Phthalocyanines 07, nr 04 (kwiecień 2003): 249–54. http://dx.doi.org/10.1142/s1088424603000331.
Pełny tekst źródłaLiang, Guodong, Jacky W. Y. Lam, Wei Qin, Jie Li, Ni Xie i Ben Zhong Tang. "Molecular luminogens based on restriction of intramolecular motions through host–guest inclusion for cell imaging". Chem. Commun. 50, nr 14 (2014): 1725–27. http://dx.doi.org/10.1039/c3cc48625g.
Pełny tekst źródłaSuzuki, Akira, Yuya Miyake, Ryoga Shibata i Kazuyuki Takai. "Spin and charge interactions between nanographene host and ferrocene". Beilstein Journal of Organic Chemistry 20 (2.05.2024): 1011–19. http://dx.doi.org/10.3762/bjoc.20.89.
Pełny tekst źródłaSun, Zhaoxi, Qiaole He, Zhihao Gong, Payam Kalhor, Zhe Huai i Zhirong Liu. "A General Picture of Cucurbit[8]uril Host–Guest Binding: Recalibrating Bonded Interactions". Molecules 28, nr 7 (31.03.2023): 3124. http://dx.doi.org/10.3390/molecules28073124.
Pełny tekst źródłaYoshida, Hiroaki, Ken Kikuta i Toshiyuki Kida. "Fabrication of supramolecular cyclodextrin–fullerene nonwovens by electrospinning". Beilstein Journal of Organic Chemistry 15 (9.01.2019): 89–95. http://dx.doi.org/10.3762/bjoc.15.10.
Pełny tekst źródłaArchana Sumohan Pillai, Sivaraj Ramasamy, Varnitha Manikandan, Aleyamma Alexander i Israel V.M.V. Enoch. "Anticancer Activity of the Host-Guest Complex of Camptothecin with β-Cyclodextrin-Folate Conjugate. Encapsulation and Efficacy". International Journal of Research in Pharmaceutical Sciences 11, SPL4 (21.12.2020): 1286–91. http://dx.doi.org/10.26452/ijrps.v11ispl4.4294.
Pełny tekst źródłaWen, Huimin, Wengang Li, Jiewei Chen, Gen He, Longhua Li, Mark A. Olson, Andrew C. H. Sue, J. Fraser Stoddart i Xuefeng Guo. "Complex formation dynamics in a single-molecule electronic device". Science Advances 2, nr 11 (listopad 2016): e1601113. http://dx.doi.org/10.1126/sciadv.1601113.
Pełny tekst źródłaRozprawy doktorskie na temat "Host-Guest moleculars"
Moncelsi, Giulia. "Stimuli-responsive host-guest systems decorated with hemithioindigo and spiropyran units". Doctoral thesis, Universitat Rovira i Virgili, 2019. http://hdl.handle.net/10803/668163.
Pełny tekst źródłaEl objetivo del trabajo de investigación incluido en esta tesis es el diseño y síntesis de sistemas receptor-huésped capaces de responder a estímulos externos. Estos sistemas cuentan con interruptores moleculares fotosensibles unidos covalentemente al receptor o al huésped. Los interruptores moleculares presentados son hemitioindigos y espiropiranos, mientras que las estructuras macrocíclicas están basadas en calix[4]arenos y calix[4]pirroles. Se estudió cómo la irradiación con luz y el tratamiento acido-base inducen la isomerización del interruptor molecular, así como el efecto que este proceso tiene en la afinidad de enlace y las propiedades de encapsulación de los receptores unimoleculares y las cápsulas supramoleculares. Se describe la síntesis de dos hemitioindigo N-oxidos. Se investigó su fotoisomerización reversible Z/E con luz visible (λ = 450 nm) al mismo tiempo que se realizó un estudio detallado de la interacción 1:1 y su efecto en la isomerización Z- y E-HTI en la cavidad aromática polar de un calix[4]pirrol super aril-extendido en disolvente orgánico. A continuación, se diseñaron y sintetizaron dos calix[4]arenos tetraurea decorados con cuatro hemitioindigos en su parte superior. Se describen los intentos de sintetizar dichos receptores y su dimerización en una variedad de disolventes orgánicos apolares y en presencia de tetrametil fosfonio. También se describe la fotoisomerización de las tetraureas en su estado monomérico y formando agregados. Finalmente, se sintetizó un calix[4]areno con unidades tetraurea capaz de responder a estímulos externos que cuenta con cuatro espiropiranos en su parte superior. Este receptor se auto ensambla formando capsulas homo- y heterodiméricas, esta última en presencia de un calix[4]pirrol similar y un N-oxido adecuado. Se discuten los estudios de auto-ensamblaje, “self-sorting”, foto- y acidocrómicos de dichos sistemas capsulares en disolventes clorados. Los resultados apuntan a que el tratamiento acido-base es reversible y predicen un buen comportamiento para su uso como transportadores y liberación de moléculas.
The aim of the research work included in this doctoral thesis is the design and synthesis of stimuli-responsive host-guest systems in which photoswitchable units are covalently incorporated into either the receptor’s or the guest’s scaffold. We use two photoswitches with distinct properties, hemithioindigos and spiropyrans, and two types of macrocyclic scaffolds based on calix[4]arene and calix[4]pyrrole. We study how light-irradiation and acid-base treatments induce the isomerization of the molecular switch. We were especially interested in coupling the isomerization processes with the binding affinity and the encapsulation properties of unimolecular receptors and supramolecular capsules, respectively. First, we describe the synthesis and photochemical characterization of two hemithioindigos featuring a terminal N-oxide moiety. We probe their Z/E reversible photoisomerization with visible light (λ = 450 nm) and we provide a detailed study of the 1:1 binding and its effect on the switching of the Z- and E-HTI isomers into the polar aromatic cavity of a super aryl-extended calix[4]pyrrole receptor in organic solvent. Next, we design and synthesize two tetraurea calix[4]arenes decorated with four hemithioindigo units at the upper rim. We describe the synthetic efforts to obtain these receptors and we investigate their dimerization in a variety of non-polar organic solvents and in the presence of tetramethyl phosphonium salts. We also report the tentative photoisomerization of the tetraureas in the monomeric state and involved in aggregates. Finally, we synthesize a stimuli-responsive tetraurea calix[4]arene featuring four appended spiropyran groups at its upper rim, which self-assembles into a homo- or heterodimeric capsule, the latter in the presence of a calix[4]pyrrole counterpart and a suitable N-oxide templating guest. The self-assembly, self-sorting, photo- and acidochromic studies of the capsular systems in chlorinated solvents are discussed. Our results suggest that the acid-base treatments are reversible and augur well for the transport and release of molecular cargo.
Bouanga, Boudiombo Jacky Sorrel. "Molecular selectivity by host-guest methods". Doctoral thesis, Faculty of Science, 2021. http://hdl.handle.net/11427/33667.
Pełny tekst źródłaBezuidenhout, Charl Xavier. "Polar ordering of guest molecules in host-guest inclusion complexes". Thesis, Stellenbosch : Stellenbosch University, 2011. http://hdl.handle.net/10019.1/18107.
Pełny tekst źródłaENGLISH 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).
Grotzfeld, Robert M. (Robert Martin). "Studies in molecular recognition : self-assembling molecular host-guest sytems". Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/10865.
Pełny tekst źródłaHOUSE, BRIAN EDWARD. "HOST-[2] ROTAXANES: GUEST RECOGNITION AND CELLULAR TRANSPORT". University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1155826127.
Pełny tekst źródłaMontalvo, Acosta Joel José. "Computational approaches to molecular recognition : from host-guest to protein-ligand binding". Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAF051/document.
Pełny tekst źródłaMolecular recognition is a very interesting problem, and foremost, a current challenge for biophysical chemistry. Having reliable predictions on the specific recognition between molecules is highly priority as it will provide an insight of fundamental problems and will raise relevant technological applications. The dissertation presented here is centered on a quantitative analysis of molecular recognition in solution for host-guest, protein-ligand binding and catalysis. The statistical mechanics framework used to describe the state-of-the-art for receptor-ligand binding is an inflection point for the developing of new improved and methods. In fact, a highly performanced and accurate model was obtained for the analysis of host-guest binding. Finally, the presented models were used as a reliable predictive tools for discovering new chemical entities for enhance catalysis in solution
MacGillivray, Leonard R. "Self-assembly for the construction of discrete and infinite host-guest architecture /". free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9924903.
Pełny tekst źródłaSMUKSTE, INESE. "ARTIFICIAL RECEPTORS FOR MOLECULAR RECOGNITION OF AMINO ACIDS, PEPTIDES AND CARBOHYDRATES". University of Cincinnati / OhioLINK, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1029757614.
Pełny tekst źródłaGarcía, Simón Cristina. "Synthesis of molecular nanocapsules for supramolecular host-guest chemistry and enzyme-like catalysis". Doctoral thesis, Universitat de Girona, 2015. http://hdl.handle.net/10803/289567.
Pełny tekst źródłaLa química d’autoacoblament dirigida per enllaços de coordinació ha facilitat l’obtenció d’una gran varietat d’estructures químiques molt sofisticades, la complexitat de les quals hagués estat molt difícil d’aconseguir mitjançant la convencional química covalent. La síntesis de càpsules de coordinació tridimensionals rep un interès especial degut a la multitud d’aplicacions que aquestes ofereixen, destacant la seva aplicació en el reconeixement selectiu de molècules (química receptor-substrat), modulació de la reactivitat (nanoreactors), sensors moleculars o les seves aplicacions biològiques. El principal objectiu d’aquesta tesi doctoral, que ha estat realitzada al grup QBIS-CAT de la Universitat de Girona, és la preparació de nanocàpsules de coordinació de diferents mides (1 i 2), i la seva aplicació en el reconeixement selectiu de substrats moleculars específics. Per una banda, la nanocàpsula més petita (1) és altament selectiva per substrats plans, aniònics amb sistemes . Per altra banda, la nanocàpsula de majors dimensions (2) pot encapsular ful·lerens de manera ràpida i a temperatura ambient, simplement amarant una mostra sòlida de la nanocàpsula en una dissolució de ful·lerens. A més, la nanocàpsula més gran es va emprar amb èxit en la separació selectiva de C60 d’una barreja de ful·lerens utilitzant un senzill protocol experimental basats en rentats del sistema nanocàpsula-ful·lerè en estat sòlid. Actualment, les aplicacions dels ful·lerens (ex. en cel·les solars o en medecina) es veuen limitades per la purificació d’aquestes molècules, que generalment s’aconsegueix mitjançant processos tediosos i costos. Els resultats d’aquesta investigació podrien facilitar el desenvolupament de noves metodologies per la purificació de barreges de ful·lerens. Finalment, la cavitat interior de la nanocàpsula de majors dimensions, 2, es va utilitzar per encapsular un catalitzador de rodi quiral que va donar alts valors de selectivitat, dels més alts que s’han observat per a un catalitzador de rodi monolligat. Els resultats obtinguts demostren que l’encapsulació del catalitzador incrementa notablement l’estereoselectivitat de la reacció, i indiquen que el confinament del catalitzador dins la caixa causa un efecte d’inducció de la selectivitat similar al que té lloc en els centres catalítics dels enzims.
Norrehed, Sara. "Modulation of Molecular Properties : Host–Guest Interactions for Structural Analysis and Chemical Reactions". Doctoral thesis, Uppsala universitet, Syntetisk organisk kemi, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-207138.
Pełny tekst źródłaKsiążki na temat "Host-Guest moleculars"
Symposium on Host-Guest Molecular Interactions: from Chemistry to Biology (1990 : Ciba Foundation), red. Host-guest molecular interactions: From chemistry to biology. Chichester: Wiley, 1991.
Znajdź pełny tekst źródłaFranco, Laeri, red. Host-guest-systems based on nanoporous crystals. Weinheim: Wiley-VCH, 2003.
Znajdź pełny tekst źródłaChadwick, Derek J., i Kate Widdows, red. Ciba Foundation Symposium 158 - Host-Guest Molecular Interactions: From Chemistry to Biology. Chichester, UK: John Wiley & Sons, Ltd., 1991. http://dx.doi.org/10.1002/9780470514085.
Pełny tekst źródłaCrowe, Declan Brendan. Macrocyclic host molecules designed to selectively bind and transport ammonium and primary ammonium guest cations. Birmingham: University of Birmingham, 1991.
Znajdź pełny tekst źródłaTite, Elizabeth Louise. The study of preorganised redox-active host molecules designed to bind neutral and cationic guest species. Birmingham: University of Birmingham, 1989.
Znajdź pełny tekst źródłaSymposium, CIBA Foundation, Derek J. Chadwick i Kate Widdows. Host-Guest Molecular Interactions: From Chemistry to Biology. Wiley & Sons, Limited, John, 2007.
Znajdź pełny tekst źródłaChadwick, Derek J., i Kate Widdows. Host-Guest Molecular Interactions: From Chemistry to Biology. Wiley & Sons, Incorporated, John, 2008.
Znajdź pełny tekst źródłaMcGuiness, C. L., R. K. Smith, M. E. Anderson, P. S. Weiss i D. L. Allara. Nanolithography using molecular films and processing. Redaktorzy A. V. Narlikar i Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.013.23.
Pełny tekst źródłaSymposium, CIBA Foundation. Host-Guest Molecular Interactions: From Chemistry to Biology - No. 158 (CIBA Foundation Symposia Series). John Wiley & Sons, 1991.
Znajdź pełny tekst źródłaCzęści książek na temat "Host-Guest moleculars"
Cram, D. J. "Designed Host-Guest Relationships". W Design and Synthesis of Organic Molecules Based on Molecular Recognition, 153–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70926-5_13.
Pełny tekst źródłaBlaschke, G. "Stereoselective Guest-Host Relationships". W Design and Synthesis of Organic Molecules Based on Molecular Recognition, 227–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70926-5_18.
Pełny tekst źródłaShinkai, Seiji. "Molecular Recognition of Calixarene-Based Host Molecules". W United States-Japan Seminar on Host-Guest Chemistry, 193–201. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0969-4_22.
Pełny tekst źródłaVögtle, Fritz, Heinz Sieger i Walter Manfred Müller. "Complexation of Uncharged Molecules and Anions by Crown-Type Host Molecules". W Host Guest Complex Chemistry / Macrocycles, 319–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70108-5_8.
Pełny tekst źródłaDearden, David V. "Host-Guest Molecular Recognition Without Solvents". W Physical Supramolecular Chemistry, 229–47. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_15.
Pełny tekst źródłaBaars, Maurice W. P. L., i E. W. Meijer. "Host-Guest Chemistry of Dendritic Molecules". W Dendrimers II, 131–82. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/3-540-46577-4_3.
Pełny tekst źródłaCheetham, A. K., i B. K. Peterson. "Computer Simulations of Host-Guest Complexes". W Inclusion Phenomena and Molecular Recognition, 277–87. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0603-0_29.
Pełny tekst źródłaSutherland, Ian O. "Molecular Recognition by Macropolycyclic Hosts". W United States-Japan Seminar on Host-Guest Chemistry, 213–26. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0969-4_24.
Pełny tekst źródłaGandour, Richard D. "Molecular Recognition in Carnitine Acyltransferases". W United States-Japan Seminar on Host-Guest Chemistry, 39–51. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0969-4_6.
Pełny tekst źródłaVinter, J. G., i M. R. Saunders. "Molecular Modelling Approaches to Host-Guest Complexes". W Novartis Foundation Symposia, 249–65. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514085.ch16.
Pełny tekst źródłaStreszczenia konferencji na temat "Host-Guest moleculars"
Singer, Kenneth D. "Optical Nonlinearities of Guest-Host-Polymer Structures". W Nonlinear Optical Properties of Materials. Washington, D.C.: Optica Publishing Group, 1988. http://dx.doi.org/10.1364/nlopm.1988.mb4.
Pełny tekst źródłaMolis, Steven E., i Robert J. Twieg. "Fourier-transform IR characterization of molecular orientation in poled polymer glasses". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.the2.
Pełny tekst źródłaIkeda, Tomiki, i Osamu Tsutsumi. "Liquid Crystalline Materials for Photonics: Optical Switching by Means of Photochemical Phase Transition of Liquid-Crystalline Azobenzene Films". W Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd63.
Pełny tekst źródłaYagyu, Eiji, Tetsuya Nishltnura i Motomu Yoshimura. "Quantitative and Theoretical Analysis of PHB-Hole Feature under Applying Electric Field." W Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.pd2.
Pełny tekst źródłaSanta María, Dolores, R. Claramunt, M. García i M. Farrán. "Molecular Modeling:Prediction of the structure of Host-Guest complexes". W The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00407.
Pełny tekst źródłaWu, J. W., J. F. Valley, M. Stiller, S. Ermer, E. S. Binkley, J. T. Kenney, G. F. Lipscomb i R. Lytel. "Poled polyimides for thermally stable electrooptic material". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oam.1991.fq4.
Pełny tekst źródłaDeeg, F. W., M. Ehrl i C. Bräuchle. "Dynamics and Guest-host Interactions of Chromophores in Inorganic Cage Structures". W Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.tub5.
Pełny tekst źródłaDogariu, Arthur, Rahul Gupta, Alan J. Heeger, Hailiang Wang, Hideyuki Murata i Zakya H. Kafafi. "Time-resolved Foerster energy transfer in molecular and polymeric guest-host systems". W SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, redaktor Zakya H. Kafafi. SPIE, 1999. http://dx.doi.org/10.1117/12.372724.
Pełny tekst źródłaSarkas, Harry W., Charles D. Merritt i Zakya H. Kafafi. "Preparation, Optical Spectroscopy, and Fluorescence of Molecular Organic Composites for Light-Emitting Diodes". W Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.md.35.
Pełny tekst źródłaIchino, Y., Y. Kanematsu i T. Kushida. "Site-Selective Excitation Spectroscopy of Dye-doped Inorganic Amorphous Hosts Prepared by Sol-Gel Method". W Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd11.
Pełny tekst źródłaRaporty organizacyjne na temat "Host-Guest moleculars"
Lawandy, Nabil M. (AASERT) Superconductors and Nonlinear Optical Materials Based on Molecular Guest-Host Systems. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1995. http://dx.doi.org/10.21236/ada299480.
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