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Relevant bibliographies by topics / Cyclopedia

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Academic literature on the topic 'Cyclopedia'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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Journal articles on the topic "Cyclopedia"

1

Stanley, Michael W. "Path-Cyclopedia." American Journal of Clinical Pathology 107, no. 4 (1997): 491.1–491. http://dx.doi.org/10.1093/ajcp/107.4.491.

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Crocker, J. "Path-cyclopedia." Molecular Pathology 50, no. 2 (1997): 112. http://dx.doi.org/10.1136/mp.50.2.112-c.

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Hayase, S. "Heibonsha, Cyclopedia of South-East Asia." Southeast Asia: History and Culture, no. 16 (1987): 155–57. http://dx.doi.org/10.5512/sea.1987.155.

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Ball, Terence, and Hal Draper. "The Marx-Engels Register: Vol. 2 of the Marx-Engels Cyclopedia." Contemporary Sociology 15, no. 3 (1986): 490. http://dx.doi.org/10.2307/2070114.

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양창진. "A Study on the Authority Centered Cyclopedia of Korean Historical Figures." Korean Cultural Studies ll, no. 75 (2017): 39–66. http://dx.doi.org/10.17948/kcs.2017..75.39.

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PARDES, I. "Remapping Jonah's Voyage: Melville's Moby-Dick and Kitto's Cyclopedia of Biblical Literature." Comparative Literature 57, no. 2 (2005): 135–57. http://dx.doi.org/10.1215/-57-2-135.

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Jefferis, G. G., and J. L. Nichols. "The Household Guide or Domestic Cyclopedia, Home Remedies for Man and Beast." Journal of Human Lactation 8, no. 2 (1992): 93–95. http://dx.doi.org/10.1177/089033449200800222.

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Augspurger, George L. "Handbook for Sound Engineers: The New Audio Cyclopedia edited by Glen Ballou." Journal of the Acoustical Society of America 83, no. 6 (1988): 2466. http://dx.doi.org/10.1121/1.396335.

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Brody, David. "Celebrating Empire on the Home Front: New York City's Welcome-Home Party for Admiral Dewey." Prospects 25 (October 2000): 391–424. http://dx.doi.org/10.1017/s0361233300000715.

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The January 3, 1900, edition of the popular, New York City newspaper the World contains an advertisement for a new edition of The Century Dictionary & Cyclopedia & Atlas (Figure 1). The strength of this reference guide, according to the full-page advertisement, is the volume's war maps. The presentation of battle cartography “enable[s] one to trace instantly the movements of every important campaign on land or sea, the routes of invading armies, raids, etc., placing and dating on the maps the battles, sieges and blockades not only of ancient and medieval times, but also those of the year just ended – and this without any complexity in the maps themselves.” In case the reader needed to be reminded about recent wars, the advertisement has enormous graphic representations of “Africa” and the “Philippine Is.” The map of the Philippines would have immediately signified the Spanish-American (1898) and Philippine-American (1899–1902) Wars to readers, conflicts that the pages of the mass media covered widely.

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Khairnar, S. B., M. V. Patil, and D. A. Patil. "Status and Development of Exotic Crops in Khandesh Region of Maharashtra (India): A Plea for Agrobiodiversity Conservation." Plantae Scientia 4, no. 4-5 (2021): 230–35. http://dx.doi.org/10.32439/ps.v4i4-5.230-235.

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Selective utilization of limited crop species threatened some other crop species. This trend rendered some crop species into underutilised grain crops throughout. At this backdrop, the present authors inventorised agrobioversity in Khandesh region of Maharashtra(India). The area was visited in different seasons. The tribal farmers were interviewed to tap down information with respect to agroclimate, yield, characteristic features etc. Actual field visits were also made in study area. The crop species were deciphered using standard state, regional and district floras, besides the manuals and cyclopedia of cultivated plants. Total 17 exotic crop species were investigated belonging to cereals, millets, pulses and edible oil-yielders. The data accrued has been evaluated with the relevant national and international scenario. A need for their conservation is earmarked with particular emphasis on underutilised millets. The subject-matter is further dilated in view of their importance for the welfare tribal people in the area and developing countries.

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Dissertations / Theses on the topic "Cyclopedia"

1

Coombs, Maurice M. "Cyclopenta[a]phenanthrenes." Thesis, University of Surrey, 1989. http://epubs.surrey.ac.uk/848494/.

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Extensive world-wide studies in cancer epidemiology throughout most of this century have led to a generally accepted view that as much as 80-90% of all human cancer has its origins in environmental factors in our diet and lifestyle. Although in most cases several factors are likely to combine to produce a particular disease, the real significance of the above conclusion is its corrollary, that identification and elimination of these environmental factors should reduce the incidence of the disease. During this time period the incidence of most forms of cancer has remained essentially constant with one notable exception, lung cancer. Mortality from this disease has risen inexorably to its present epidemic proportions during the last seventy years and now accounts for the death of some 26000 men and 15 000 women each year in England and Wales alone. There is now no doubt that this is a direct result of cigarette smoking, and it is reliably predicted that abandonment of the habit would reduce this death rate ten-fold. The causes of other major forms of cancer, such as breast cancer in women and colon cancer in both sexes, have proved to be much more elusive. Their origins are probably complex and they are more difficult to study because there are no natural 'controls' as there are with lung cancer, where direct comparisons may be made between smokers and non-smokers. All possibilities for their causation are now under active consideration, and among them the influence of endogenous carcinogens generated by aberrant metabolism within the host is unknown, but cannot be discounted. It is now established that carcinogens of varied types are elaborated by both plants and microorganisms, and there seems to be no a priori reason why animals should not be similarly afflicted. Since most cancers are primarily diseases of old age it would seem unlikely that there would be strong evolutionary pressure against this happening. The idea that carcinogens, arising from steroids by incorrect metabolism, might be important in the induction of human cancer was a view commonly held in the past, but which has been neglected in recent times. Over fifty years ago, at the very outset of research into chemical carcinogenesis, the potent poly cyclic aromatic hydrocarbon carcinogen 3-methylcholanthrene was prepared by simple chemical transformations from a bile acid derivative. The correct structures for the bile acids and sterols were themselves established at about the same time, and the synthesis of this carcinogen took on an exaggerated importance in the minds of scientists. The enduring idea that methylcholanthrene formed by incorrect bile acid or sterol metabolism in the body might prove to be a cause of human cancer led to numerous attempts to identify this carcinogen in tumours and other tissues, but without success. The reason for this failure now seems obvious because experience has shown that cyclization of the sterol side chain does not occur to provide a fifth fused ring. Instead this side-chain tends to be lost with migration of the angular methyl groups, leading to compounds of the simpler four-ring cyclo-penta[a]phenanthrene series. These compounds thus possess the same basic carbon ring system as the steroids, but lack the angular methyl groups which characterize the latter. They are therefore capable of complete dehydrogenation to fully aromatic phenanthrene derivatives, and compounds of this type do in fact occur widely in petroleum and in oil-bearing shales as well as in river and lake sediments; they are also found in cooking oils that have been overheated. Advances in our understanding of oestrogen biosynthesis and metabolism have moreover suggested a plausible route by which cyclopenta[a]phenanthrenes might be formed in the body, but so far no attempts have been made to test this possibility. The need for further investigations in this area using modern techniques is now apparent, because numerous cyclopenta[a]phenan-threnes have since been synthesized and some have been shown to be strong carcinogens, similar in potency to the classical poly cyclic hydrocarbon carcinogen benzo[a]pyrene. This book is concerned with the occurrence, chemical synthesis, physical and chemical properties, and biological attributes of cyclo-penta[a]phenanthrenes. These are discussed in detail, as is their history which is intimately connected with the establishment of the correct structure of steroids. Interesting structure /carcinogenicity relationships, similar to those found among related polycyclic aromatic systems such as the chrysenes and benzo[a]anthracenes, are examined in relation to the metabolism of these compounds and the interactions of their metabolites with biological macromolecules. The book also lists physical data for nearly 350 cyclopenta[a]phenanthrene derivatives and contains exhaus- tive references to the original literature. It is hoped that it will provide a useful point of departure for those concerned with the possibility of the involvement of cyclopenta[a]phenanthrenes in the aetiology of human disease.

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Güllük, Eduard. "Synthese von Cyclopenta[c]pyran-3(5H)-on und Cyclopenta[c]pyran-3(7H)-on als Vorstufen von Cyclopenta[c]pyranen." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969694067.

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Hofmann, Thorsten. "Synthese und Reaktionen von Cyclopenta[c]1,2-diazepinen und Cyclopenta[d]1,2-diazepinen." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=963775774.

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Lee, Katherine Lin. "Synthetic approach to cyclopenta[alpha]phenalene." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/39061.

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Lee, Che-Hsiung. "ORTHOGONAL FUNCTIONALIZATION OF CYCLOPENTA[HI]ACEANTHRYLENES." OpenSIUC, 2014. https://opensiuc.lib.siu.edu/theses/1542.

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This thesis is based on a research project aimed at the selective modification of the known cyclopenta-fused polycyclic aromatic hydrocarbon (CP-PAH) based electron acceptor cyclopenta[hi]aceanthrylene. Starting form 2,7-bis(trimethylsilyl)cyclopenta-[hi]aceanthrylene, we utilized bromination and/or C-H activation strategies that could orthogonally functionalize the cyclopenta[hi]aceanthrylene core. Depending on which reagents were utilized, aromatic substitutions could be directed to either the five-membered rings or the six-membered rings. The functionalization location had dramatic effects on the resulting material's optical band gap with the highest occupied molecular orbital being most affected. We further demonstrate how these materials are good electron acceptors through cyclic voltammetry as well as a fluorescence quenching experiments with poly(3-hexylthiophene). Lastly, we have extended the described functionalization strategy to dicyclopenta[de,mn]tetracene based CP-PAHs.

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Boyd, Gary William. "Cyclopenta[a]phenanthren-17-ones : structure/activity relationships." Thesis, University of Surrey, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334403.

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Karambelkar, Vineet V. "Proposed Route to Cyclopenta[c]thiophenes via Activated Methylene." TopSCHOLAR®, 2008. http://digitalcommons.wku.edu/theses/25.

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The synthesis of cyclopenta[c]thiophenes has been sparsely reported in the literature owing to several difficulties involved in their synthesis. The present work involves the proposed synthesis of cyclopenta[c]thiophenes and their precursors using activated methylene. Cyclopenta[c]thiophene compounds show promise in the field of polymer and catalysis chemistry. These substituted polythiophenes are potential organic semiconductors and anti-tumor agents. The research presented shows the successful and novel conversion of 3,4-bis(chloromethyl)-2,5-dimethylthiophene and 3,4-bis(bromomethyl)-2,5-dimethylthiophene to a fused 5,5'-fused membered ring which is the precursor to cyclopenta[c]thiophene the sulfone ester, 5-carbomethoxy-5- phenylsulfonyl-1,3-dimethyl-5,6-dihydro-4H-cyclopenta[c]thiophene, in just two steps as compared to four steps previously reported in the literature. This valuable precursor intermediate currently made and proven by characterization is one synthetic step away from a substituted cyclopenta[c]thiophene. A paper has been submitted to Letters in Organic Chemistry to report our work.

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Grandin, Anna. "Synthetic Routes towards 2-thia-7,8-diaza-cyclopenta[l]phenanthrene and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene for Molecular Electronics Applications." Thesis, Mälardalens högskola, Akademin för hållbar samhälls- och teknikutveckling, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-7505.

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Electric current is known to flow through the π-bonds in oligothiophenes. In order to use them as molecular wires it is important to use a technique where the potential gradients can be generated and maintained in supramolecular networks. A solution to this problem can be the use of metal complexes as junction points within such a network. In this project pathways to synthesize 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) for use in molecular electronic devices have been investigated. 4-(5-Bromo-thiophen-2-yl)2,2’-bipyridine (3) was prepared via Kröhnke reaction from 3-(5-bromothiophene-2-yl)acrolein and 1-(2-Oxo-2-pyridine-2-yl-ethyl)-pyridinium iodide in an overall yield of 14 %. Several routes towards 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) were tested. Since the original planned pathway did not work, lack of time made it impossible to complete the series of experiments that were needed. The synthesis of 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) is almost finished. Due to the solvation problems, after the decarboxylation step, the product could not be analyzed by 1H-NMR in a satisfactory manner. The product was sent for analysis. A number of experiments towards 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) were tested but few of them worked as planned. There is a lot of work left to be done in the synthesis of this compound but the lack of time made it impossible. The chemistry that has been achieved is the synthesis of 1,10-phenanthroline-5,6-dione in the synthesis of 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1). The following Hinsberg thiophene synthesis probably worked but due to solvation problems the product could not be isolated. The final product after hydrolysis and decarboxylation of the remaining ester groups after the Hinsberg thiophene synthesis was tested but the results were difficult to confirm. In the synthesis of 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) several attempts to make 3,4-diamino-N,N-diethyl-benzamide were made. The attack from the primary amines on the carbonyl carbon made it necessary to protect them. The attempt to synthesize 3,4-bis-acetylamino-N,N-diethyl-benzamide also failed, both the attempt directly from the carboxylic acid and through the acylchloride, even though the amines were protected.

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Bell, Amber. "A Modified Route to Cyclopenta[C]Thophenes Via Grignard Reagents." TopSCHOLAR®, 2007. http://digitalcommons.wku.edu/theses/963.

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The synthesis of cyclopenta[c]thiophenes is sparsely found in literature due to the several difficulties of their synthesis. Our research has shown that we could modify a previously known route to 1,3-disubstituted cyclopenta[c]thiophenes using traditional Grignard chemistry. Along the way we discovered the synthetic route we were using had several omissions. Therefore, we were required to completely fill in missing experimentals in order to obtain each cyclopenta[c]thiophene intermediate, in high purity and good yield. In addition, we were able to fully characterize via NMR, our intermediates which was found in the literature. Finally, we were able to show using 'H 13 and 13C NMR spectroscopy evidence of 5-alkyl-l,3-disubstituted cyclopenta[c]thiophenes by treating l,3-dimethyl-5,6-dihydro-4H-cyclopenta[c]thio-phene-5-one with an alkyl Grignard reagent. 1 A ser1i3e s of cyclopenta[c]thiophene intermediates will be presented along with their H and C NMR spectra. A discussion of cyclopenta[c]thiophene synthesis will be provided along with attempts to improve its experimental conditions. A paper has been submitted to Letters in Organic Chemistry to report our work.

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Rigby, Suzie S. "Sigmatropic and haptotropic shifts in complexes of cyclopenta(l)phenanthrene." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0020/NQ30185.pdf.

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Books on the topic "Cyclopedia"

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Phillips, Shaun. MTV-cyclopedia. Carlton, 1997.

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The nautical cyclopedia. G. Gentile Productions, 1995.

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Samuel, Loyd. Cyclopedia of puzzles. Ishi Press International, 2007.

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Vaknin, Shmuel (Sam). Cyclopedia of Philosophy. Narcissus Publications, 2007.

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Vaknin, Shmuel (Sam). Cyclopedia of Economics. 3rd ed. Narcissus Publications, 2009.

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1854-1943, Hart Albert Bushnell, Ferleger Herbert Ronald 1914-, and Gable John A, eds. Theodore Roosevelt cyclopedia. 2nd ed. Theodore Roosevelt Association, 1989.

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Suren. Cyclopedia of Yoga. Saru Pub. House, 1992.

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Center for Socialist History (Berkeley, Calif.), ed. The Marx-Engels cyclopedia. Schocken Books, 1985.

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J, Sobczak A., Long Janet Alice, and Magill Frank Northen 1907-, eds. Cyclopedia of literary characters. Salem Press, 1998.

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Love, Richard H. Cyclopedia of American impressionism. Brittenham-Mumm, 2007.

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Book chapters on the topic "Cyclopedia"

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Yeh, Catherine Vance. "Helping Our People “to Jointly Hurry Along the Path to Civilization.” The Everyday Cyclopedia, Riyong baike quanshu 日用百科全書." In Transcultural Research – Heidelberg Studies on Asia and Europe in a Global Context. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35916-3_11.

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Rudebusch, Gabriel E., and Michael M. Haley. "Planar Cyclopenta-Fused Polycyclic Arenes." In Polycyclic Arenes and Heteroarenes. Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527689545.ch2.

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Vogt, J. "700 C8H9N 6,7-Dihydro-5H-cyclopenta[b]pyridine." In Asymmetric Top Molecules. Part 3. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_122.

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Nian, Jiazhen, Shan Jiang, Congrui Huang, and Yan Zhang. "CCE: A Chinese Concept Encyclopedia Incorporating the Expert-Edited Chinese Concept Dictionary with Online Cyclopedias." In Advanced Data Mining and Applications. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-25853-4_16.

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Winkelmann, Jochen. "Diffusion coefficient of bi-(4H-cyclopenta[def]phenenthren-4-ylidene) in tetrahydro-furan-d8." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1022.

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Winkelmann, Jochen. "Diffusion coefficient of 4,4'-bi-1H-cyclopenta[def]phenanthrene ion(2-) in tetrahydro-furan-d8." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1023.

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Blake, Paul C., Michael F. Lappert, Richard C. Taylor, Paulette N. Hazin, and Joseph W. Bruno. "Bis[η5 -1, 3-Bis(Trimethylsilyl)Cyclopenta-Dienyl]Halouranium(IV) and-Thorium(IV), [MCp″2 Cl2 ] and [UCp″2 X2 ]." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132586.ch34.

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Pasalic, Ademir, Nikolaj Hollænder Andersen, Christopher Schinkel Carlsen, Emil Åberg Karlsson, Markus Berthold, and Thomas Bjørner. "How to Increase Boys’ Engagement in Reading Mandatory Poems in the Gymnasium: Homer’s “The Odyssey” as Transmedia Storytelling with the Cyclopeia Narrative as a Computer Game." In Smart Objects and Technologies for Social Good. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-76111-4_22.

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Lappert, Michael F., Anirudh Singh, and Josef Takats. "Bis[η5 -1, 3-Bis(Trimethylsilyl)Cyclopenta-Dienyl]Chlorolanthanide(III) Complexes, [{LnCp″2 (μ-Cl)}2 ] and [LnCp″2 Gi-Cl)2 Li(thf)2 ]." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132586.ch33.

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"Oak." In The Liberty Hyde Bailey Gardener's Companion, edited by John A. Stempien and John Linstrom. Cornell University Press, 2019. http://dx.doi.org/10.7591/cornell/9781501740237.003.0018.

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The poetic entry for the term "Oak" from Bailey's Standard Cyclopedia of Horticulture is offered here. The oak "connects the present with the past. It spans the centuries." As elsewhere, the poetic and the scientific merge in this essay about this commonly known tree species.

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Conference papers on the topic "Cyclopedia"

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Suh, Hongsuk, Youngeup Jin, Suhee Song, Changjin Yoo, and Jaehong Kim. "Efficient blue organic light-emitting diodes with 4H-cyclopenta[def]phenanthrene." In Photonic Devices + Applications, edited by Zakya H. Kafafi and Franky So. SPIE, 2007. http://dx.doi.org/10.1117/12.730990.

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Blanco, José, Paula Abeijón, Olga Caamaño, Franco Fernández, Marcos García, and Xerardo García-Mera. "A convenient synthesis of new 6-substituted purinylcarbanucleosides on cyclopenta[b]thiophene." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01238.

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Ghildina, A. R., A. M. Mebel, and V. N. Azyazov. "The oxidation of cyclopenta[b]naphthalene C13H9 radical at the combustion conditions." In INTERNATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF COMBUSTION AND PROCESSES IN EXTREME ENVIRONMENTS (COMPHYSCHEM’20-21) and VI INTERNATIONAL SUMMER SCHOOL “MODERN QUANTUM CHEMISTRY METHODS IN APPLICATIONS”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0033820.

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Takesue, Tomoko. "Abstract 5190: Detection of radioresistant gene of esophageal cancer by the new cyclopedic gene analysis with transposon." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-5190.

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Gangjee, Aleem, Weiguo Xiang, Susan L. Mooberry, and Ernest Hamel. "Abstract 1665: Design, synthesis, biological evaluation of cyclopenta[d]pyrimidines as antitubulin agents and discovery of N-(4-methylthiophenyl) and N-(4-dimethylaminophenyl) substituted N,2-dimethyl-cyclopenta[d]pyrimidines as long acting and poten." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1665.

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Fernandes, D. C., R. N. S. Santos, M. T. R. Júnior, A. D. Andricopulo, and F. Coelho. "Discovery and synthesis of a new analogues of the cyclopenta[b]indoles as tubulin polymerization inhibitors." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013103173553.

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Toussaint, J. M., and J. L. Bredas. "Geometric and electronic structures of polydicyanomethylene-cyclopenta-dicyclopentadiene, a conjugated polymer possessing a very small intrinsic bandgap energy." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.836143.

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Khasanov, Albert F., Dmitry S. Kopchuk, Alexey P. Krinochkin, et al. "2,7-diehtynyl-10-(pyridin-2-yl)-12,13-dihydro-11H-dibenzo[f,h]cyclopenta[c]quinoline as potential monomer for creating polymers for different tasks." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018783.

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Lee, Te-Chang, Pei-Chih Lee, Rajesh Kakadiya, and Tsann-Long Su. "Abstract C31: Derivatives of 3a-aza-cyclopenta[a]indene effectively suppress the growth of P-glycoprotein overexpressing cells in in vitro and in vivo systems." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-c31.

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Huang, Jen Wei, Ming Seng Hsu, and Tzu-Chin Lin. "Organic photovoltaic cells of fully conjugated poly[2,6- (4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b';]dithiophene)-alt-4,7-(2,1,3-benzothiadiazole)] doped with fullerene." In SPIE Optical Engineering + Applications, edited by Shizhuo Yin and Ruyan Guo. SPIE, 2014. http://dx.doi.org/10.1117/12.2060787.

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