Bibliografías temáticas / Macrocycles

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Literatura académica sobre el tema "Macrocycles"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de julio de 2025

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Artículos de revistas sobre el tema "Macrocycles"

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Abdelraheem, Eman, Shabnam Shaabani, and Alexander Dömling. "Artificial Macrocycles." Synlett 29, no. 09 (2018): 1136–51. http://dx.doi.org/10.1055/s-0036-1591975.

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Artificial macrocycles recently became popular as a novel research field in drug discovery. As opposed to their natural twins, artificial macrocycles promise to have better control on synthesizability and control over their physicochemical properties resulting in druglike properties. Very few synthetic methods allow for the convergent, fast but diverse access to large macrocycles chemical space. One synthetic technology to access artificial macrocycles with potential biological activity, multicomponent reactions, is reviewed here, with a focus on our own work. We believe that synthetic chemist
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Singh, Kartikey, and Rama Pati Tripathi. "An Overview on Glyco-Macrocycles: Potential New Lead and their Future in Medicinal Chemistry." Current Medicinal Chemistry 27, no. 20 (2020): 3386–410. http://dx.doi.org/10.2174/0929867326666190227232721.

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Macrocycles cover a small segment of molecules with a vast range of biological activity in the chemotherapeutic world. Primarily, the natural sources derived from macrocyclic drug candidates with a wide range of biological activities are known. Further evolutions of the medicinal chemistry towards macrocycle-based chemotherapeutics involve the functionalization of the natural product by hemisynthesis. More recently, macrocycles based on carbohydrates have evolved a considerable interest among the medicinal chemists worldwide. Carbohydrates provide an ideal scaffold to generate chiral macrocycl
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Zhong, Chunxiao, Yong Yan, Qian Peng, et al. "Structure–Property Relationship of Macrocycles in Organic Photoelectric Devices: A Comprehensive Review." Nanomaterials 13, no. 11 (2023): 1750. http://dx.doi.org/10.3390/nano13111750.

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Macrocycles have attracted significant attention from academia due to their various applications in organic field-effect transistors, organic light-emitting diodes, organic photovoltaics, and dye-sensitized solar cells. Despite the existence of reports on the application of macrocycles in organic optoelectronic devices, these reports are mainly limited to analyzing the structure–property relationship of a particular type of macrocyclic structure, and a systematic discussion on the structure–property is still lacking. Herein, we conducted a comprehensive analysis of a series of macrocycle struc
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Fan, Linmeng, Min Du, Lichun Kong, Yan Cai, and Xiaobo Hu. "Recognition Site Modifiable Macrocycle: Synthesis, Functional Group Variation and Structural Inspection." Molecules 28, no. 3 (2023): 1338. http://dx.doi.org/10.3390/molecules28031338.

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Traditional macrocyclic molecules encode recognition sites in their structural backbones, which limits the variation of the recognition sites and thus, would restrict the adjustment of recognition properties. Here, we report a new oligoamide-based macrocycle capable of varying the recognition functional groups by post-synthesis modification on its structural backbone. Through six steps of common reactions, the parent macrocycle (9) can be produced in gram scale with an overall yield of 31%. The post-synthesis modification of 9 to vary the recognition sites are demonstrated by producing four di
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Guo, Hao, Yu-Fei Ao, De-Xian Wang, and Qi-Qiang Wang. "Bioinspired tetraamino-bisthiourea chiral macrocycles in catalyzing decarboxylative Mannich reactions." Beilstein Journal of Organic Chemistry 18 (May 2, 2022): 486–96. http://dx.doi.org/10.3762/bjoc.18.51.

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A series of tetraamino-bisthiourea chiral macrocycles containing two diarylthiourea and two chiral diamine units were synthesized by a fragment-coupling approach in high yields. Different chiral diamine units, including cyclohexanediamines and diphenylethanediamines were readily incorporated by both homo and hetero [1 + 1] macrocyclic condensation of bisamine and bisisothiocyanate fragments. With the easy synthesis, gram-scale of macrocycle products can be readily obtained. These chiral macrocycles were applied in catalyzing bioinspired decarboxylative Mannich reactions. Only 5 mol % of the op
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Sun, Dianqing. "Recent Advances in Macrocyclic Drugs and Microwave-Assisted and/or Solid-Supported Synthesis of Macrocycles." Molecules 27, no. 3 (2022): 1012. http://dx.doi.org/10.3390/molecules27031012.

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Macrocycles represent attractive candidates in organic synthesis and drug discovery. Since 2014, nineteen macrocyclic drugs, including three radiopharmaceuticals, have been approved by FDA for the treatment of bacterial and viral infections, cancer, obesity, immunosuppression, etc. As such, new synthetic methodologies and high throughput chemistry (e.g., microwave-assisted and/or solid-phase synthesis) to access various macrocycle entities have attracted great interest in this chemical space. This article serves as an update on our previous review related to macrocyclic drugs and new synthetic
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Kim, Taegwan, Eunbee Baek, and Jonghoon Kim. "Exploring Macrocyclic Chemical Space: Strategies and Technologies for Drug Discovery." Pharmaceuticals 18, no. 5 (2025): 617. https://doi.org/10.3390/ph18050617.

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Macrocycles have emerged as significant therapeutic candidates in drug discovery due to their unique capacity to target complex and traditionally inaccessible biological interfaces. Their structurally constrained three-dimensional configurations facilitate high-affinity interactions with challenging targets, notably protein–protein interfaces. However, despite their potential, the synthesis and optimization of macrocyclic compounds present considerable challenges related to structural complexity, synthetic accessibility, and the attainment of favorable drug-like properties, particularly cell p
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Li, Yu, Wei Zhao, and Biao Wu. "Tetraurea Macrocycles: Template-Directed One-Pot Synthesis and Anion Binding Properties." Advances in Engineering Technology Research 6, no. 1 (2023): 228. http://dx.doi.org/10.56028/aetr.6.1.228.2023.

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Given the significance of anion in life, study of anion recognition attracted great attentions in the past decades. Macrocyclic receptors display intriguing anion binding properties; however, the synthesis of macrocycles is challenging. Here, we reported a new strategy of making tetraurea in one-step. By using 1-butyl-3-methylimidazolium ([hmim][X], X = anion) as the solvent and template reagent, tetraurea macrocycle comprised of bis(urea) binding moiety and hexyl chain spacers is selectively formed with high yield. The obtained macrocycles displayed interesting anion binding properties as ind
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Chia, PSK, A. Ekstrom, I. Liepa, et al. "New Macrocyclic Ligands. II. Pendant Hydroxyethyl, Cyanoethyl and Carbamoylethyl Arm Systems Derived From O2N2-Donor Rings: the X-Ray Structure of a Pendant Hydroxyethyl Derivative." Australian Journal of Chemistry 44, no. 5 (1991): 737. http://dx.doi.org/10.1071/ch9910737.

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The syntheses and characterization of 12 new 14- to 17-membered macrocycles incorporating pendant hydroxyethyl cyanoethyl or carbamoylethyl groups are reported. The macrocyclic ring in each of these new ligands contains an O2N2-donor set. The X-ray structure of the di(hydroxyethyl) derivative of the 14-membered macrocycle is described.
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Mohammed, Shaymaa Adil. "Synthesis and Characterization of Some New Polymeric Macrocycle (Thia-Crown Ether) and Study Biological Activity." International Journal of Medical and All Body Health Research 6, no. 2 (2025): 87–98. https://doi.org/10.54660/ijmbhr.2025.6.2.87-98.

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This study investigates the synthesis, characterization, and biological activity of novel polymeric thia-crown ethers. On of the best solutions to save time and costs by mobilizing the chiral macrocycles on polymers which allows the recyclability and green conditions, The selecting of glucose as a model for the synthesis of macrocyclic thia crown ether The synthesis of thia-crown ether is started with protection of 4,6-positions on methyl D-glucopyranoside 1 by benzylidene protecting group, the reaction of compound 2 with bis(2-chloroethyl)ether under basic conditions to get compound 3 to obta
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Tesis sobre el tema "Macrocycles"

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Azarias, Cloé. "Modeling azacalixphyrin macrocycles." Thesis, Nantes, 2018. http://www.theses.fr/2018NANT4021/document.

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Cette thèse porte sur la modélisation des propriétés structurales, aromatiques et spectroscopiques d'une nouvelle classe de macrocycles alternatifs aux porphyrines, les azacalixphyrines (ACPs). Ces macrocycles conjugués, synthétisés et caractérisés pour la première fois en 2010 par le groupe d’Olivier Siri à Marseille, ont montré des propriétés exceptionnelles (structure, absorption, tautomérie, et complexation). Cette thèse vise à proposer de nouveaux dérivés aux propriétés améliorées, notamment en ce qui concerne leur absorption, en utilisant les outils offerts par la chimie théorique. Parmi
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Danso-Danquah, Richmond Edward. "Syntheses of polypyrrolic macrocycles." Thesis, University of British Columbia, 1986. http://hdl.handle.net/2429/26240.

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Pentaphyrins are pentapyrrolic macrocycles containing five bridging methine groups between the five pyrrolic subunits. The syntheses of decamethylpentaphyrin 71, 2-ethoxycarbonyl-3,7,8,12,13,17,18,22,23-nonamethylpentaphyrin 74, 2-ethoxycarbonyl-3,7,8,22,23-pentamethyl-12,13,17,18-tetraethylpentaphyrin 75, 3,12-dimethoxycarbonylethyl-2,7,8,-13,17,18,22,23-octamethylpentaphyrins 29 and the zinc complexes of 71 and 74 are described. The physical properties of the pentaphyrins show them to be aromatic like sapphyrins, porphyrins and corroles. This aromaticity is reflected in the large shielding
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Norman, Timothy John. "Radioimmunotherapy with yttrium macrocycles." Thesis, Durham University, 1994. http://etheses.dur.ac.uk/5529/.

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Monoclonal antibody fragments (Fab') which recognise tumour-associated antigens provide an ingenious means of selectively targeting a therapeutic radionuclide to a tumour for radioimmunotherapy. The radionuclide yttrium-90, a long range β(^-) emitter, was chosen to deliver a sterilising dose of radiation to the tumour. A selection of novel functionalised macrocyclic ligands based on a 1,4,7,10-tetraazacyclododecane skeleton have been synthesised, and the stabilities of their yttrium (III) and gadolinium (III) complexes studied in vitro through association and dissociation measurements, and in
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Matthes, Karen Elizabeth. "Chemistry of functionalised macrocycles." Thesis, Durham University, 1987. http://etheses.dur.ac.uk/6704/.

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The work reported in this thesis is divided into two distinct areas. The first involves the synthesis of monoaza- and diaza-[12]-ring macrocycles, with differing side-arm N-substituents. The twelve-membered macrocycles possess a convenient ring-size for exploring the stability and selectivity of complexation of small cations, in particular those from groups IA and IIA. Amide substituents on nitrogen were expected to function as effective σ-donors to cations with high charge density (e.g. Li (^+), Ca (^2)(^+)), because of their high ground state dipole moments. The effect of the length of the s
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Sloman, Zachary Scott. "Novel thiophene based macrocycles." Thesis, Nottingham Trent University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297724.

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Marrs, Deborah Jane. "Macrocycles, macrobicycles : a study." Thesis, Open University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257447.

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Colombo-Khater, Dominique. "Macrocycles polyhétéroatomiques : synthèse, complexation." Toulouse 3, 1993. http://www.theses.fr/1993TOU30001.

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Depuis quelques annees, de nombreux macrocycles phosphores contenant des heteroatomes ont ete prepares dans le but d'obtenir des especes capables de complexer selectivement des cations voire meme des especes neutres. La methode de synthese mise au point au laboratoire en 1988 consiste a faire reagir un dialdehyde sur un phosphodihydrazide. Il s'agit d'une methode simple et generale de synthese de macrocycles polyphosphores. La reaction mise en jeu est une reaction de cyclocondensation 2+2. L'etude bibliographique presentee dans le premier chapitre nous a permis de faire le point sur les differ
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Watson, Walter Philip. "Hybrid Macrocycles for Supramolecular Assemblies." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/6958.

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Hybrid macrocycles, which chimerically integrate multiple chemical compositions and architectures, provide an effective way to impart new properties to polymers that are not found in their linear or homocyclic analogues. This dissertation addresses the incorporation of hydrophilic blocks into hydrophobic polymer, as either a poly(dimethyl siloxane)-block-poly(oxyethylene) (PDMS-POE) tadpole with a hydrophobic head and a hydrophilic tail or as a diblock poly(styrene)-block-diethylene glycol (PS-DEG) hydrophobic-hydrophilic macrocycle. The supramolecular association properties of both kinds of
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Morphy, John Richard. "Functionalised macrocycles for tumour targeting." Thesis, Durham University, 1988. http://etheses.dur.ac.uk/6407/.

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Monoclonal antibodies which recognise tumour-associated antigens provide a means of targeting radionuclides selectively to tumour cells. (^99m)Tc and (^64)Cu are potentially useful isotopes for radioimmunoimaging;(^ 90)Y and (^67)Cu may be suitable for radioimmunotherapy. The synthesis of functionalised macrocycles for binding these four radioisotopes to antibodies is described. In each case, a macrocycle has been selected to provide a complex which is kinetically inert, thereby preventing dissociation of the radiolabel in vivo. A novel strategy for conjugating a C-alkylated cyclam derivative
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Wood, Ian. "Hydrogen bonded double helical macrocycles." Thesis, University of Nottingham, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285635.

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Libros sobre el tema "Macrocycles"

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Davis, Frank, and Séamus Higson. Macrocycles. John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470980200.

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E, Weber, Vögtle F. 1939-, and Burrell A. K, eds. Macrocycles. Springer-Verlag, 1992.

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Coppock, Matthew B., and Alexander J. Winton, eds. Peptide Macrocycles. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1689-5.

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Bradshaw, J. S. Aza-crown macrocycles. Wiley, 1993.

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Levin, Jeremy, ed. Macrocycles in Drug Discovery. Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781782623113.

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Kim, Kimoon, ed. Cucurbiturils and Related Macrocycles. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015967.

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Marsault, Eric, and Mark L. Peterson, eds. Practical Medicinal Chemistry with Macrocycles. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119092599.

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Vögtle, Fritz, and Edwin Weber, eds. Host Guest Complex Chemistry / Macrocycles. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70108-5.

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Ball, Melissa Lynne. Conjugated Macrocycles in Organic Electronics. [publisher not identified], 2019.

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Campbell, Paul James. Towards macrocycles with interactive functional groups. University ofBirmingham, 1994.

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Capítulos de libros sobre el tema "Macrocycles"

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Yao, Huan, and Wei Jiang. "Naphthol-Based Macrocycles." In Handbook of Macrocyclic Supramolecular Assembly. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2686-2_40.

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Yao, Huan, and Wei Jiang. "Naphthol-Based Macrocycles." In Handbook of Macrocyclic Supramolecular Assembly. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1744-6_40-1.

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Mamedov, Vakhid A. "Synthesis of Quinoxaline Macrocycles." In Quinoxalines. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29773-6_5.

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Wessjohann, Ludger A., Ricardo A. W. Neves Filho, Alfredo R. Puentes, and Micjel Chávez Morejón. "Macrocycles from Multicomponent Reactions." In Practical Medicinal Chemistry with Macrocycles. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119092599.ch14.

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Masson, Géraldine, Luc Neuville, Carine Bughin, Aude Fayol, and Jieping Zhu. "Multicomponent Syntheses of Macrocycles." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/7081_2010_47.

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Sellers, Benjamin D., Brian R. Hearn, Katerina Leftheris*, and Jennifer X. Qiao. "MACROCYCLES IN DRUG DISCOVERY." In Medicinal Chemistry Reviews. MEDI, Inc. Published by American Chemical Society., 2024. http://dx.doi.org/10.1021/mc-2024-vol59.ch15.

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Wessjohann, Ludger A., Ricardo A. W. Neves Filho, Alfredo R. Puentes, and Micjel C. Morejon. "Macrocycles from Multicomponent Reactions." In Multicomponent Reactions in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527678174.ch09.

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Chio, Weng-I. Katherine, and Tung-Chun Lee. "Host–Guest Chemistry of Macrocycles." In Macrocycle-Functionalised Nanosensors. Jenny Stanford Publishing, 2024. http://dx.doi.org/10.1201/9781003510574-2.

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Ronson, Thomas O., William P. Unsworth, and Ian J. S. Fairlamb. "Palladium-Catalyzed Synthesis of Macrocycles." In Practical Medicinal Chemistry with Macrocycles. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119092599.ch12.

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Wessjohann, Ludger A., Richard Bartelt, and Wolfgang Brandt. "Natural and Nature-Inspired Macrocycles." In Practical Medicinal Chemistry with Macrocycles. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119092599.ch4.

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Actas de conferencias sobre el tema "Macrocycles"

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Rajan, K. S., P. Sen, E. J. Vesely, S. Verma, V. S. Agarwala, and A. A. Conte. "Macrocyclic Compounds for Corrosion-Wear." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90444.

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Abstract The possible application of Schiff base compounds as corrosion- and wear-protective additives in lubricant formulations suitable for use at high temperatures (i.e., ≥200 °C) has been investigated. In addition to their planar structure and quadridentate metal-binding characteristics similar to those of the macrocyclic compounds such as the phthalocyanines and porphyrins, the Schiff base compounds exhibit appropriate thermal stabilities. Lubricant formulations using selected Schiff base compounds, phthalocyanines and porphyrins were prepared and tested for their corrosion protection and
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Hettiarachchi, S., Y. W. Chan, R. B. Wilson, and V. S. Agarwala. "Macrocyclic Corrosion Inhibitors for Steel in Acid Chloride Environments." In CORROSION 1987. NACE International, 1987. https://doi.org/10.5006/c1987-87223.

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Abstract The effectiveness of phthalocyanines as acid corrosion inhibitors for steel have been studied. Water soluble tetrasulfophthalocyanines are very poor corrosion inhibitors. Water insoluble tetraaminophthalocyanines serve as better corrosion inhibitors than the water soluble ones when the metal surface is coated with an adsorbed layer of the phthalocyanine. The inhibitor efficiency was still far too low to be of any significance. Water insoluble polymeric phthalocyanine coatings based on Fe(III) centers gave inhibitor efficiencies as high as 82%, as confirmed by both slow potentiodynamic
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Janak, Kevin E., Steven Colby, Tre Bertrand, and Brittany Fontenot. "Development of an Asphaltene Deposit Cleaning Technology Using a QCMB Technique." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12821.

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Absrract Asphaltenes are a components of crude oil defined as a solubility class, i.e., as a component of crude oil insoluble in n-pentane (C5 asphaltenes) or n-heptane (C7 asphaltenes) but soluble in aromatic solvents such as toluene, and are complex, polyaromatic, macrocyclic structures with an overall varied composition. Asphaltene deposition, remediation, and inhibition are important considerations for flow assurance in upstream processes, but methodologies to assess performance for cleaning purposes can provide variable results. We report on the development of a dispersant additive for ar
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Shutalev, Anatoly, Anastasia Fesenko, Dmitry Albov, Vladimir Chernyshev, and Ilia Zamilatskov. "Novel 14-Membered Hexaaza Macrocycles." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a042.

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Gill, Hubert S., Michael Harmjanz, and Michael J. Scott. "Porphodimethenes/porphyrins: redox-switchable tetrapyrrolic macrocycles." In Complex Adaptive Structures, edited by William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446774.

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Ortiz-Jimenez, Orlando, Mónica Trejo-Durán, Edgar Alvarado-Méndez, Israel Severiano-Carrillo, and Egla Bivian-Castro. "Macrocycles in sol-gel matrix: nonlinear optical characterization." In SPIE Nanoscience + Engineering, edited by Stefano Cabrini, Gilles Lérondel, Adam M. Schwartzberg, and Taleb Mokari. SPIE, 2016. http://dx.doi.org/10.1117/12.2238228.

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Dimova, Iva. "STUDY OF STRENGTH TRAINING IN FEMALE 400 m SPRINT EVENT IN AGE ASPECT." In INTERNATIONAL SCIENTIFIC CONGRESS “APPLIED SPORTS SCIENCES”. Scientific Publishing House NSA Press, 2022. http://dx.doi.org/10.37393/icass2022/07.

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ABSTRACT Studying the different aspects of 400 m sports preparation is a key factor for the proper development of sports results. Strength training is one of the main pillars of sprint running. The object of the study is sports training of athletes in the 400 m sprint, and in particular strength training. The subject is the content and volume of the annual preparation for different age groups. We used the following methods: sports-pedagogical and technical-tactical analysis of athletes; interviews with coaches and athletes; Case-study analysis; Mathematical and statistical methods. A total of
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Rella, R., L. Valli, and F. Chetta. "Optical sensing through wide delocalised macrocycles by SPR technique." In Proceedings of the 6th Italian Conference. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812810779_0012.

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Kepenekian, Mikael, Auguste Tetenoire, Arnaud Fihey, and Corinne Lagrost. "Covalent anchoring of macrocycles on metallic nanoparticles for electrocatalysis." In MATSUS Spring 2025 Conference. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2024. https://doi.org/10.29363/nanoge.matsusspring.2025.197.

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Leif, Robert C., Margie C. Becker, Lidia M. Vallarino, John W. Williams, and Sean Yang. "Progress in the use of Quantum Dye Eu(III)-macrocycles." In Biomedical Optics 2003, edited by Dan V. Nicolau, Joerg Enderlein, Robert C. Leif, and Daniel L. Farkas. SPIE, 2003. http://dx.doi.org/10.1117/12.486324.

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Informes sobre el tema "Macrocycles"

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van Swol, Frank B., and Craig John Medforth. Structural simulations of nanomaterials self-assembled from ionic macrocycles. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1008138.

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Root, Harrison Duane. Applications of Porphyrinoid Macrocycles in Molecular Sensing and f-Element Coordination. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1635507.

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McKenna, Gregory, Julia Kornfield, and Judit Puskas. Polymer Macrocycles: A novel topology to control dynamics of rubbery materials. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1971136.

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McKenna, Gregory, Julia Kornfield, and Judit Puskas. Polymer Macrocycles: A novel topology to control dynamics of rubbery materials. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1958282.

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Puskas, Judit. Polymer Macrocycles: A novel topology to control dynamics of rubbery materials. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/2203196.

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Allcock, Harry R. Strained Inorganic Heterocyclic Compounds and their Conversion to Macrocycles and High Polymers. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada241414.

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Puskas, Judit, Gregory McKenna, and Julia Kornfield. Collaborative Research: Polymer Macrocycles: A novel topology to control dynamics of rubbery materials. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1654432.

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Eyring, Edward M., and Sergio Petrucci. Rates and Mechanisms of Complexation Reactions of Cations with Crown Ethers and Related Macrocycles. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada203436.

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Klumpp, Doug Allen. The intramolecular cyclization of bis-2,5-dimethylene-2,5-dihydrofurans and bis-2,5-dimethylene-2,5-dihydrothiophenes: An approach to macrocycles. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10125330.

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Potts, K. Macrocyclic ligands for uranium complexation. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7201376.

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