Relevant bibliographies by topics / Anthraquinone Derivative

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Anthraquinone Derivative'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Anthraquinone Derivative"

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Anderson, Benjamin R., and Mark G. Kuzyk. "Imaging studies of photodegradation and self-healing in anthraquinone derivative dye-doped PMMA." Physical Chemistry Chemical Physics 22, no. 48 (2020): 28154–64. http://dx.doi.org/10.1039/d0cp05426g.

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We compare the photodegradation and self-healing properties of nine anthraquinone derivatives doped into PMMA using transmission imaging. The results suggests “rules-of-thumb” to predict enhanced photostability and self-healing for anthraquinones.
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Caballero, Ana B., Nikolas J. Hodges, and Michael J. Hannon. "Folate-Receptor-Targeted Gold Nanoparticles Bearing a DNA-Binding Anthraquinone." Inorganics 13, no. 3 (2025): 87. https://doi.org/10.3390/inorganics13030087.

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In recent years, anthraquinones have been widening their therapeutic opportunities given their numerous health benefits. The search for adequate delivery platforms to improve their pharmacokinetics leads us to propose herein folate-capped gold nanoparticles with an anthraquinone derivative attached onto their surface. Through a straightforward, two-step procedure, we obtained stable nanoparticles that can deliver anthraquinones selectively to cells overexpressing folate receptors. The new conjugates were highly toxic against two tumour cell lines, lung carcinoma A549 and cervical carcinoma HeL
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Li, Xin, Xiao-Ming Li, and Bin-Gui Wang. "Structural Revision of Wentiquinone C and Related Congeners from Anthraquinones to Xanthones Using Chemical Derivatization and NMR Analysis." Marine Drugs 17, no. 1 (2018): 8. http://dx.doi.org/10.3390/md17010008.

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Wentiquinone C, which was previously isolated from the marine brown alga-derived endophytic fungus Aspergillus wentii EN-48, was found to be a potent antioxidant against α,α-diphenyl-picrylhydrazyl (DPPH) radical. The structure of wentiquinone C was originally assigned as an anthraquinone derivative (1,10-dihydroxy-3-(hydroxymethyl)-8-methoxydibenzo [b,e]oxepine-6,11-dione, 1) by 1D and 2D NMR experiments. However, the minor differences of the chemical shifts between xanthones and anthraquinones were queried, leading to the structure of 1 to be revised as a xanthone analog (8-hydroxy-6-(hydrox
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Rehman, ATA Ur, Shahid Ali, Safyan Akram Khan, and Muhammad Mansha. "Tuning the Performance of Anthraquinone-Derived Anolytes for AORFBS." ECS Meeting Abstracts MA2025-01, no. 45 (2025): 2416. https://doi.org/10.1149/ma2025-01452416mtgabs.

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Aqueous organic redox flow batteries (AORFBs) have garnered more recent interest because of their cost benignity, safety and suitable performance. In this regard, anthraquinone-based anolytes have proven capabilities under various conditions. Many derivatives of the anthraquinones have been opted to get an optimum performance for the low-cost redox flow batteries. Herein, we have first introduced a new derivative of the anthracenedione as an anolyte in the aqueous redox flow battery. The AORFB comprising 0.1 M of this anolyte, and coupled with the potassium hexaferrocyanide (0.2 M), has shown
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Ge, Xueping, Chunxiao Sun, Yanyan Feng, et al. "Anthraquinone Derivatives from a Marine-Derived Fungus Sporendonema casei HDN16-802." Marine Drugs 17, no. 6 (2019): 334. http://dx.doi.org/10.3390/md17060334.

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Five new anthraquinone derivatives, auxarthrols D–H (1–5), along with two known analogues (6–7), were obtained from the culture of the marine-derived fungus Sporendonema casei. Their structures, including absolute configurations, were established on the basis of NMR, HRESIMS, and circular dichroism (CD) spectroscopic techniques. Among them, compound 4 represents the second isolated anthraquinone derivative with a chlorine atom, which, with compound 6, are the first reported anthraquinone derivatives with anticoagulant activity. Compounds 1 and 3 showed cytotoxic activities with IC50 values fro
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Miki, Sadao, Hiroyuki Kagawa, and Zen-Ichi Yoshida. "Chemiexcitation of an anthraquinone derivative in the thermal cycloreversion of a dewar-anthraquinone derivative." Journal of Physical Organic Chemistry 5, no. 2 (1992): 101–3. http://dx.doi.org/10.1002/poc.610050206.

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Yang, Xiaowei, Yinhuan Zhang, Yan Liu, Chang Chen, Wenjuan Xu, and Hongbin Xiao. "Emodin induces liver injury by inhibiting the key enzymes of FADH/NADPH transport in rat liver." Toxicology Research 7, no. 5 (2018): 888–96. http://dx.doi.org/10.1039/c7tx00307b.

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Kazmi, Mehdi H., Abdul Malik, Saira Hameed, Nargis Akhtar, and Samina Noor Ali. "An anthraquinone derivative from Cassia italica." Phytochemistry 36, no. 3 (1994): 761–63. http://dx.doi.org/10.1016/s0031-9422(00)89812-x.

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Hosoe, Tomoo, Koohei Nozawa, Shun-ichi Udagawa, Shoichi Nakajima, and Ken-ichi Kawai. "An anthraquinone derivative from Dichotomophthora lutea☆." Phytochemistry 29, no. 3 (1990): 997–99. http://dx.doi.org/10.1016/0031-9422(90)80068-r.

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Zhao, Huan, Zhiqun He, Min Xu, Chunjun Liang, and Sandeep Kumar. "Electron transporting organic materials with an exceptional large scale homeotropic molecular orientation." Physical Chemistry Chemical Physics 18, no. 12 (2016): 8554–60. http://dx.doi.org/10.1039/c6cp00031b.

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Dissertations / Theses on the topic "Anthraquinone Derivative"

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Alam, Zohaib. "Anti-Cytomegalovirus Activity of Atanyl Blue PRL, an Anthraquinone Derivative." VCU Scholars Compass, 2013. http://scholarscompass.vcu.edu/etd/3166.

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Cytomegalovirus (CMV) is a significant cause of mortality and morbidity in immunocompromised patients and an important cause of birth defects if acquired in utero. The licensed CMV antivirals, ganciclovir, cidofovir and foscarnet, all target the viral DNA polymerase. For each drug prolonged use is associated with significant toxicities and development of drug resistance. None are approved for use during pregnancy. Therefore, development of new anti-CMV drugs that target different pathways would be beneficial. All herpesviruses encode an alkaline nuclease. That genetic disruption of the CMV alk
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Alaparthi, Madhubabu. "Molecular Recognition Involving Anthraquinone Derivatives and Molecular Clips." Thesis, University of South Dakota, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10285748.

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<p> In the past, we have demonstrated that 1,8-anthraquinone-18-crown-5 (1) and its heterocyclic derivatives act as luminescent hosts for a variety of cations of environmental and clinical concern. We report here a series of heteroatom-substituted macrocycles containing an anthraquinone moiety as a fluorescent signaling unit and a cyclic polyheteroether chain as the receptor. Sulfur, selenium, and tellurium derivatives of 1,8-anthraquinone-18-crown-5 (<b>1</b>) were synthesized by reacting sodium sulfide (Na<sub>2</sub>S), sodium selenide (Na<sub>2</sub>Se) and sodium telluride (Na<sub>2</sub>
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Argade, A. B. "Synthesis of biologically active anthraquinone derivatives via marschalk reaction." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1988. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3308.

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Abou-Elkhair, Reham A. I. "Synthesis of anthraquinone derivatives and their conjugates with 2'-deoxynucleosides as new probes for electron transfer studies in DNA." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-07182008-154942/.

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Thesis (Ph. D.)--Georgia State University, 2008.<br>Title from file title page. Thomas L. Netzel, Dabney W. Dixon, committee co-chairs; David Boykin, Jerry Smith, committee members. Electronic text (250 p. : ill. (some col.)) : digital, PDF file. Description based on contents viewed Nov. 20, 2008. Includes bibliographical references.
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Ma, Jiani, and 马佳妮. "Time-resolved spectroscopic studies of meta methyl activation reaction of selected benzophenone and anthraquinone derivatives." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/196012.

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Femtosecond time-resolved transient absorption (fs-TA), nanosecond time-resolved transient absorption (ns-TA), and nanosecond time-resolved resonance Raman spectroscopy (ns-TR3) methods were used to study the behaviors of the transient intermediates involved in the photophysical and photochemical processes of 3-methylbenzophenone (3-MeBP), 3-(hydroxymethyl)benzophenone (m-BPOH), and 2-(1-hydroxyethyl) 9,10-anthraquinone (2-HEAQ). A particular focus of this work was to study the unusual meta methyl activation reactions of these compounds in water-containing solutions. Density functional theor
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Ezenwafor, E. I. I. "The synthesis and properties of derivatives of 1-amino-4-hydroxy anthraquinone : The synthesis of thiolated derivatives of 1-amino-4-hydroxy anthraquinone and a study of their application, dyeing and fastness properties on synthetic-polymer fibres." Thesis, University of Bradford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371494.

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Cao, Yu. "I. Synthesis Of Anthraquinone Derivatives For Electron Transfer Studies In DNA. II. Characterization Of The Interaction Between Heme And Proteins." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/55.

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Anthraquinone (AQ) derivatives with relatively high reduction potentials have been synthesized to afford good candidates for electron transfer studies in DNA. Electron withdrawing groups on the anthraquinone ring gave derivatives with less negative reduction potentials. The anthraquinone imide (AQI) derivatives had reduction potentials less negative than AQ derivatives. The AQI ring system was subject to base-induced hydrolysis. Water-soluble sulfonated tetraarylporphyrins have been studied in a wide variety of contexts. Herein, we report the first synthesis of a pentasulfonated porphyrin
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Oliveira, Larissa Albuquerque de. "Preparação, caracterização e avaliação de novos análogos da mitoxantrona com potenciais atividades biológicas." Universidade Federal de Juiz de Fora (UFJF), 2017. https://repositorio.ufjf.br/jspui/handle/ufjf/5893.

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Submitted by Renata Lopes (renatasil82@gmail.com) on 2017-10-11T14:54:00Z No. of bitstreams: 1 larissaalbuquerquedeoliveira.pdf: 6821961 bytes, checksum: e1edff2fb674ae0aef7703387d259bf8 (MD5)<br>Approved for entry into archive by Adriana Oliveira (adriana.oliveira@ufjf.edu.br) on 2017-10-16T13:50:15Z (GMT) No. of bitstreams: 1 larissaalbuquerquedeoliveira.pdf: 6821961 bytes, checksum: e1edff2fb674ae0aef7703387d259bf8 (MD5)<br>Made available in DSpace on 2017-10-16T13:50:15Z (GMT). No. of bitstreams: 1 larissaalbuquerquedeoliveira.pdf: 6821961 bytes, checksum: e1edff2fb674ae0aef7703387d259
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HSU, CHIN-CHIA, and 許晉嘉. "The Role of SIRT1 in Regulating Chemoresistance of a Novel Anthraquinone Derivative in Prostate Cancer Cells." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/9u6xw4.

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碩士<br>慈濟大學<br>生命科學系碩士班<br>105<br>SIRT1, the mammalian homologue of the silent information regulator 2 (Sir2) gene which belongs to the family of type III histone deacetylase, is implicated in diverse cellular processes including cell survival under genotoxic and oxidative stresses. SIRT1 expression is correlated with cell growth, as well as the chemoresistance, and is markedly up-regulated in androgen-refractory prostate cancer PC3 cells. SIRT1-induced autophagy is known to occur at the level of autophagosome maturation and completion in cultured prostate cancer cells. To identify novel small
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Wei-Ren, Jeng, and 鄭維仁. "Synthesis and Bioactivity Evaluation of 1,5-Bis-acyloxy-anthraquinone and 1,5-Bis-thio-substituted Anthraquinone Derivatives." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/03785161358076035167.

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碩士<br>國防醫學院<br>藥學研究所<br>89<br>We have synthesized 23 compounds of anthraquinone derivatives, which included 1,5-bis-acyloxy-anthraquinone and 1,5-bis-thio-substituted anthraquinone. We wish to choose more active compounds by cytotoxic tests and lipid-peroxidation tests. Now we have three compounds more active than mitoxantrone against Hepa G2 cells (about 5 to 85 times stronger), and they are compound 5b、5f、5m; in addition, one compound, 6a, is more active than mitoxantrone against C6 glioma cells (about > 3.5 times stronger). In the lipid-peroxidation test, we concluded that at 10 mM, compoun
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Books on the topic "Anthraquinone Derivative"

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Ezenwafor, Ephraim Ifeanyi Ihechukwu. The synthesis and properties of derivatives of 1-amino-4-hydroxy anthraquinone: The synthesis ofthiolated derivatives of 1-amino-4-hydroxyanthraquinone and a study of their application, dyeing and fastness properties on synthetic-polymer fibres. 1985.

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Book chapters on the topic "Anthraquinone Derivative"

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Sparapano, L., P. Lerario, and G. Anelli. "Production of Anthraquinone Derivatives by Phoma Tracheiphila." In Phytotoxins and Plant Pathogenesis. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-73178-5_38.

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Chen, Zujie, Suyi Liu, Xiangbo Sun, Jingyun Wu, Hongbo Zhu, and Runjin Zhu. "The biochemical effects of rhubarb extract's six anthraquinone derivatives in treating lung cancer." In Advances in Applied Chemistry and Industrial Catalysis. CRC Press, 2022. http://dx.doi.org/10.1201/9781003308553-15.

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Kumar, Vasantha, Prashasthi V. Rai, Ganavi D., Vijesh A. M., and Roopa Nayak. "Anthraquinone Derivatives as Potent Anti-Cancer Agents." In Anthraquinones: Bioactive Multifaceted Therapeutic Agents. BENTHAM SCIENCE PUBLISHERS, 2025. https://doi.org/10.2174/9789815313987125030007.

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Cancer is one of the high-mortality-causing diseases in the world. It causes a serious threat to mankind with an estimated 10 million deaths every year. Identifying novel drug candidates for the treatment of various types of cancer is a prime research area in medicinal chemistry. Even though many drug molecules are used in cancer treatment, they suffer from various drawbacks, such as low selectivity, toxicity, and resistance to new tumor cells. Hence, the search for novel anti-cancer agents is a continuous process in order to develop more efficient and less toxic chemotherapeutic agents. Among
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Sharma, Pooja, and Amrit Kaur. "An Overview of Chemistry and Biosynthesis of Anthraquinones." In Anthraquinones: Bioactive Multifaceted Therapeutic Agents. BENTHAM SCIENCE PUBLISHERS, 2025. https://doi.org/10.2174/9789815313987125030005.

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Anthraquinones are a class of secondary metabolites, have garnered significant interest due to their diverse biological activities and various industrial applications. The derivatives of anthraquinones are widely distributed in nature, being found in numerous plants, fungi, and bacteria. The biosynthetic pathways leading to anthraquinones differ among various organisms, yet common underlying mechanisms can be observed. Enzymatic reactions play a pivotal role in the functionalization and diversification of anthraquinones. Cytochrome P450 monooxygenases, glycosyltransferases, and acyltransferase
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Siddiqui, Mohd Aftab, Mohammad Saidur Rahman, Anas Islam, Afreen Usmani, and Usama Ahmad. "Emodin: Anticancer Agent." In Frontiers in Clinical Drug Research - Anti-Cancer Agents. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223910124090007.

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Cancer is a serious health issue that remains a significant cause of mortality around the world. Psychosocial support, surgery, radiation, and chemotherapy are common cancer treatments. However, because of the rising rate of cancer-related mortality and the adverse or toxic side effects of cancer chemotherapy and radiation therapy, new anticancer compounds obtained from nature, particularly plants, are currently being researched. Phytochemicals, which are naturally occurring plant substances, are important sources for new drugs and cancer treatment. Phytochemicals are selective in their action
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"Carbonyl Dyes and Pigments." In Colour Chemistry, 2nd ed. The Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/bk9781849733281-00099.

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The chemical class of colorants that is second in importance to azo dyes and pigments is characterized by the presence of a carbonyl (CO) group, which may be regarded as the essential chromophoric unit. A substantial part of this chapter is devoted to anthraquinones, the most important group of carbonyl dyes and pigments. In contrast to azo dyes, carbonyl dyes are found in nature; dyes such as indigo and alizarin – an anthraquinone derivative – are amongst the most important natural dyes for textiles. Synthetic carbonyl dyes and pigments are capable of providing a wide range of colours, essen
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Celik, Sefa, Funda Ozkok, Sevim Akyuz, and Aysen E. Ozel. "The Importance of Anthraquinone and Its Analogues and Molecular Docking Calculation." In Computational Models for Biomedical Reasoning and Problem Solving. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-7467-5.ch007.

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In drug-delivery systems containing nano-drug structures, targeting the tumorous tissue by anthraquinone molecules with high biological activity, and reaching and destroying tumors by their tumor-killing effect reveals remarkable results for the treatment of tumors. The various biological activities of anthraquinones and their derivatives depend on molecular conformation; hence, their intra-cell interaction mechanisms including deoxyribonucleic acid (DNA), ribonucleic acid (RNA), enzymes, and hormones. Computer-based drug design plays an important role in the design of drugs and the determinat
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"Study of light-induced interaction of quinone derivatives with guanosine and guanosine-rich oligonucleotides." In Book of Abstracts - RAD 2025 Conference. RAD Centre, Niš, Serbia, 2025. https://doi.org/10.21175/rad.abstr.book.2025.6.3.

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Quinones are a broad class of compounds of both synthetic and natural origin that are actively used in medicine, particularly in anticancer therapy. Their main mechanism of cytotoxicity is associated with interaction with DNA. This type of interaction is possible due to the flat aromatic system of quinones. Model processes of interaction of the naphthoquinone derivative N-(2-chloro-1,4- naphthoquinonyl)-b-alanine (Nap) as well as the anthraquinone 2-phenyl-4-(butylamino)- naphtholquinoline-7,12-dione (Q1) with 5'-guanidylic acid (GMP) and oligonucleotide sequences of different lengths (2G, 3G,
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KAWAGUCHI, Yoshihisa. "OPTICAL PERSISTENT HOLE BURNING OF ANTHRAQUINONE DERIVATIVES." In Computer Aided Innovation of New Materials. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-444-88864-8.50105-9.

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Stasevych, M. V., and V. I. Zvarych. "9,10-anthraquinone derivatives as new promising antimicrobial compounds." In ACHIEVEMENTS OF UKRAINE AND THE EU IN ECOLOGY, BIOLOGY, CHEMISTRY, GEOGRAPHY AND AGRICULTURAL SCIENCES. Izdevnieciba “Baltija Publishing”, 2021. http://dx.doi.org/10.30525/978-9934-26-086-5-46.

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Conference papers on the topic "Anthraquinone Derivative"

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Fu, Liwu, Lisheng Zheng, and Yan-yan Yan. "Abstract 4400: Blockade of Her2 binding to Hsp90 by emodin azide methyl anthraquinone derivative induces proteasomal degradation of Her2." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4400.

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Yagyu, Eiji, Tetsuya Nishimura, and Motomu Yoshimura. "Persistent Hole Burning and Holography in Anthraquinone Derivatives." In Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd57.

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We have reported persistent spectral hole burning (PHB) in anthraquinone derivatives. 1-3) Hole burning spectroscopy desires high resolution to detect narrow and shallow holes. Laser induced grating (Holography) technique is very effective for the investigation of a shallow hole, because it enables to detect a small signal without a large background. 4-6) In addition, we can achieve many holographic applications: 3D image storage and reconstruction, holographic memory, holographic computing, etc. However, we should note that hole signal represents a diffraction efficiency in holographic detect
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Alwi, Ratna Surya, Kazuhiro Tamura, Tatsuro Tanaka, and Keisuke Shimizu. "Solubility correlation of anthraquinone derivatives in supercritical carbon dioxide." In INTERNATIONAL SEMINAR ON FUNDAMENTAL AND APPLICATION OF CHEMICAL ENGINEERING 2016 (ISFAChE 2016): Proceedings of the 3rd International Seminar on Fundamental and Application of Chemical Engineering 2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4982328.

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Anderson, Benjamin, Shiva K. Ramini, and Mark G. Kuzyk. "Imaging studies of photodamage and recovery of anthraquinone derivatives doped into PMMA." In XLIII Annual Symposium on Optical Materials for High Power Lasers, edited by Gregory J. Exarhos, Vitaly E. Gruzdev, Joseph A. Menapace, Detlev Ristau, and M. J. Soileau. SPIE, 2011. http://dx.doi.org/10.1117/12.896369.

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Yoday, B. C. "Optical and electrical properties of anthraquinone derivatives : work in the last 8 years." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835526.

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Yagyu, Eiji, Tetsuya Nishltnura, and Motomu Yoshimura. "Quantitative and Theoretical Analysis of PHB-Hole Feature under Applying Electric Field." In Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.pd2.

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We have investigated the stark effect on the spectral hole characteristics in the photochemical hole burning systems of anthraquinone derivatives, such as, 1,4-dihydroxyanthraquinone (HAQ) and 4-amino-2,6-bis(4-butylphenoxy)1,5-dihydroxyanthraquinone (ABDAQ) as guest molecules embedded in host polymers such as 2-hydroxyethyl methacrylate (PHEMA) or poly(vinyl butyral) (PVB)1-3). Consequently, we evaluated the dipole moment differences |δμ| of guest molecules. These dipole moment differences depended on the characteristics of the guest and host molecules. This material dependence of the dipole
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Kelber, O., S. Haßler, K. Jung, B. Feistel, B. Steinhoff, and K. Nieber. "Studies of herbal drug preparations containing anthraquinone derivatives in the Ames test: No hints on mutagenicity." In GA – 70th Annual Meeting 2022. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1759316.

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Zhou, Manxi, Zhimin Sun, Guangxin Chen, and Qifang Li. "Synthesis of Perylene Bisimide Derivatives and Poly(Triphenylamine-Block-Anthraquino) for Polymer Photovoltaics." In 2011 Asia-Pacific Power and Energy Engineering Conference (APPEEC). IEEE, 2011. http://dx.doi.org/10.1109/appeec.2011.5748418.

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Dhakal, P., S. K. Ramini, and Mark G. Kuzyk. "Correlation between molecular structure and self-healing in a series of Anthraquinone derivatives doped in PMMA polymer." In SPIE Optical Engineering + Applications, edited by Edward W. Taylor, David A. Cardimona, Ronald G. Pirich, Narasimha S. Prasad, Javier Pérez-Moreno, and Nathan J. Dawson. SPIE, 2012. http://dx.doi.org/10.1117/12.929424.

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