Thematische Bibliographien / Organic groups

Inhaltsverzeichnis

  1. Zeitschriftenartikel
  2. Dissertationen
  3. Bücher
  4. Buchteile
  5. Konferenzberichte
  6. Berichte der Organisationen

Auswahl der wissenschaftlichen Literatur zum Thema „Organic groups“

Autor: Grafiati
Veröffentlicht am 18. Mai 2024
Zuletzt aktualisiert am 26. Juli 2025

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Zeitschriftenartikel zum Thema "Organic groups"

1

Yamamoto, Katsutoshi, Yuki Nohara, Yusuke Domon, et al. "Organic−Inorganic Hybrid Zeolites with Framework Organic Groups." Chemistry of Materials 17, no. 15 (2005): 3913–20. http://dx.doi.org/10.1021/cm048367g.

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Wan, Ying, Dieqing Zhang, Na Hao, and Dongyuan Zhao. "Organic groups functionalised mesoporous silicates." International Journal of Nanotechnology 4, no. 1/2 (2007): 66. http://dx.doi.org/10.1504/ijnt.2007.012316.

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Saleh, Asmaa Najeeb Ahmad, Khadija Nasser Mohammed Noori, Saja Huusin Ali Sulamin, Ghufran Kadhum Abed Hasan, and Qahtan Adnan Jassim Mohammad. "PROTECTING GROUPS FOR ORGANIC SYNTHESIS." European Journal of Medical Genetics and Clinical Biology 1, no. 7 (2024): 111–35. http://dx.doi.org/10.61796/jmgcb.v1i7.739.

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A protecting group (English protecting group - therefore often referred to as common abbreviation in formula schemes PG) is in chemistry a substituent which, during a more complicated, multi-step chemical synthesis in a molecule is introduced to a specific functional group to protect temporarily and so an undesirable reaction to prevent this group. After the desired reaction has been carried out elsewhere on the molecule, the protective group is split off again. For many functional groups several possible protective groups are known which differ in their stability and the conditions for their
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Hodge, P. "Protective groups in organic synthesis." Polymer 33, no. 16 (1992): 3542. http://dx.doi.org/10.1016/0032-3861(92)91123-j.

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Wilson, A. J. C. "Space groups rare for organic compounds." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (1987): C289. http://dx.doi.org/10.1107/s0108767387077717.

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Dral, A. Petra, and Johan E. ten Elshof. "Organic groups influencing microporosity in organosilicas." Microporous and Mesoporous Materials 267 (September 2018): 267–73. http://dx.doi.org/10.1016/j.micromeso.2018.03.036.

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Creyghton, Edward J. "Organic groups cling to the pores." Nature 393, no. 6680 (1998): 21–22. http://dx.doi.org/10.1038/29886.

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8

Surtiningsih, Tini, Fatimah Fatimah, Ni’matuzahroh Ni’matuzahroh, Agus Supriyanto, and Tri Nurhariyati. "PELATIHAN PEMBUATAN PUPUK ORGANIK CAIR PADA KELOMPOK TANI DI KABUPATEN PROBOLINGGO." Jurnal Layanan Masyarakat (Journal of Public Services) 2, no. 1 (2020): 21. http://dx.doi.org/10.20473/jlm.v2i1.2018.21-24.

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This community service aims to apply the method of making and liquid organic fertilizer and improving the skills of farmers in making liquid organic fertilizer. In addition to reducing the dependence of farmer groups on inorganic fertilizers and utilizing the results of sugarcane waste, namely molasses and microbes as a formula in the manufacture of liquid organic fertilizer. The method that was carried out was to increase insight into liquid organic fertilizer, and how to make it. The results of the socialization of liquid organic fertilizers showed that the insights of farmer groups increase
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Ravikumar, Velayutham, Andrea Fin, Naomi Sakai, and Stefan Matile. "Solubilising groups: a conceptual equivalent of protecting groups in organic synthesis." Supramolecular Chemistry 23, no. 1-2 (2010): 69–73. http://dx.doi.org/10.1080/10610278.2010.510193.

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Wilson, A. J. C. "Space groups rare for organic structures. Erratum." Acta Crystallographica Section A Foundations of Crystallography 45, no. 2 (1989): 210. http://dx.doi.org/10.1107/s0108767388014205.

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Dissertationen zum Thema "Organic groups"

1

Dunlop, J. E. "Coordinated leaving groups in organic synthesis." Thesis, Bucks New University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.374820.

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Mouselmani, Rim. "Reduction of Organic Functional Groups Using Hypophosphites." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSE1241/document.

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Récemment, les exigences en chimie ont évolué rapidement, car le développement durable a retenu plus d'attention. Les principes de la chimie verte ont encouragé les chimistes à développer des produits chimiques et des procédés qui réduisent ou éliminent les substances dangereuses. Les travaux de recherche décrits dans cette thèse portent sur le développement de nouveaux systèmes réducteurs en utilisant des hypophosphites comme substituts aux agents réducteurs toxiques traditionnels.Pour atteindre cet objectif, les nitriles aromatiques ont été réduits en aldéhydes correspondants par la formatio
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Nomura, Glenn Sterling. "Derivatives of 4-ketoperhydroazulene with bridgehead methyl groups." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/27064.

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Lee, Duckhee. "The design of organosilyl groups to control organic reactions." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624740.

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5

Ahmed, K. M. "Diels-Alder reaction of quinones carrying electron-withdrawing groups." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234154.

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6

Hussain, Firasat [Verfasser]. "Hybrid organic-inorganic polyoxometalates functionalized by diorganotin groups / Firasat Hussain." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2008. http://d-nb.info/1034891162/34.

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Longstaff, Peter A. "Novel side chain protecting groups for solid phase peptide synthesis." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/15232.

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Korzycka, Karolina Anna. "Two-photon sensitive protecting groups for biological application." Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:7e895ed2-04a5-4c0b-9105-74461eae8796.

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Caged compounds are a class of photosensitive reagents used to stimulate cells with spatial control down to a sub-cellular level, and millisecond temporal control. They comprise of biologically important molecule which is modified with a photolabile protecting group. In the absence of light, caged compounds are physiologically silent but irradiation with light induces the release of biologically active species. Illumination under two-photon conditions is particularly advantageous as it enables restriction of the photolysis volume to ~1 fL and it provides deeper penetration into scattering samp
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He, Chaobin. "Synthesis and structure of rigid chain polyamides with bulky side groups." Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/273003.

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Deodhar, Bhushan S. "Towards the development of rotaxanes with two functional blocking groups." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1311690891.

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Bücher zum Thema "Organic groups"

1

McOmie, J. F. W., ed. Protective Groups in Organic Chemistry. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4684-7218-9.

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2

M, Wuts Peter G., ed. Protective groups in organic synthesis. 3rd ed. Wiley, 1999.

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Greene, Theodora W. Protective groups in organic synthesis. 2nd ed. Wiley, 1991.

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Wuts, Peter G. M., ed. Greene's Protective Groups in Organic Synthesis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118905074.

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Gordon, Hanna J., ed. Quantitative organic analysis via functional groups. 4th ed. R.E. Krieger Pub. Co., 1988.

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R, Katritzky Alan, Meth-Cohn Otto, Rees Charles W, and Pattenden Gerald, eds. Comprehensive organic functional group transformations. Pergamon, 1995.

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R, Katritzky Alan, Meth-Cohn Otto, Rees Charles W, and Gilchrist T. L, eds. Comprehensive organic functional group transformations. Pergamon, 1995.

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R, Katritzky Alan, Meth-Cohn Otto, Rees Charles W, and Ley Steven V, eds. Comprehensive organic functional group transformations. Pergamon, 1995.

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9

Lemke, Thomas L. Review of organic functional groups: Introduction to medicinal organic chemistry. 2nd ed. Lea & Febiger, 1988.

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Lemke, Thomas L. Review of organic functional groups: Introduction to medicinal organic chemistry. 3rd ed. Lippincott Williams & Wilkins, 1999.

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Buchteile zum Thema "Organic groups"

1

Sarker, Satyajit D., and Lutfun Nahar. "Organic Functional Groups." In Chemistry for Pharmacy Students. John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118687529.ch4.

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2

Boons, G. J. "Protecting Groups." In Organic Synthesis with Carbohydrates. Sheffield Academic Press Ltd, 2008. http://dx.doi.org/10.1002/9780470760321.ch2.

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3

Gutman, Ivan, and Oskar E. Polansky. "Automorphism Groups." In Mathematical Concepts in Organic Chemistry. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70982-1_10.

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Gutman, Ivan, and Oskar E. Polansky. "Symmetry Groups." In Mathematical Concepts in Organic Chemistry. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70982-1_9.

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5

Burgess, D. A. "Organic Chemistry — Functional Groups." In Work Out Chemistry ‘A’ Level. Macmillan Education UK, 1987. http://dx.doi.org/10.1007/978-1-349-24067-8_12.

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Tucker, William B. "Common Organic Functional Groups and Nomenclature." In Organic Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-27.

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Vančik, Hrvoj. "Functional Groups." In Basic Organic Chemistry for the Life Sciences. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07605-8_2.

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Vančik, Hrvoj. "Functional Groups." In Basic Organic Chemistry for the Life Sciences. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92438-6_2.

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Saunders, K. J. "Other Aromatic Polymers Containing p-Phenylene Groups." In Organic Polymer Chemistry. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1195-6_12.

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Carey, Francis A., and Richard J. Sundberg. "Reactions of Carbon Nucleophiles with Carbonyl Groups." In Advanced Organic Chemistry. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_2.

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Konferenzberichte zum Thema "Organic groups"

1

Knorr, Erica S., Jordan C. Kelly, Daniel P. Harrison, and Thomas N. Rohrabaugh. "Effect of electron-donating and -withdrawing groups on the photophysical properties of iridium (iii) diphenyl quinoxaline complexes." In Organic Photonic Materials and Devices XXVII, edited by Ileana Rau, Okihiro Sugihara, and William M. Shensky. SPIE, 2025. https://doi.org/10.1117/12.3047905.

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2

Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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Haskaj, Adelina, Musaj Pacarizi, Sonja Lepitkova, Berat Sinan, Bahri Sinani, and Elida Dreshaj. "THE POTENTIAL COMPLEXING IMPACT OF SOME ORGANIC COMPOUNDS AMINE AND CARBOXYL GROUPS ON TRANSITION METALS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s18.42.

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Environmental water chemistry is substantially aided by modern electrochemical research. Sensitive voltammetric techniques are much more useful for metal species in natural waters, where complexation with organic molecules predominates. Many environmental electrochemists are still interested in determining the stability constants of metal ion complexes with various ionic species found in natural waterways. The aim of this work is to investigate the possible influence of complexation of amine and carboxyl groups of some organic molecules (with EDTA, NTA and aniline, using differential pulse pol
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Samariks, Valters, Ieva Jaunslaviete, Andis Adamovics, Sabine Dubasinska, and Aris Jansons. "GROUND VEGETATION BIOMASS AND CARBON POOL IN HEMIBOREAL OLD-GROWTH CONIFEROUS STANDS ON ORGANIC SOILS." In 24th SGEM International Multidisciplinary Scientific GeoConference 2024. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/3.2/s13.36.

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Forest ground vegetation biomass plays a significant role in carbon (C) storage and contributes to the overall carbon pool of forest ecosystems. Ground vegetation, including understory plants, shrubs, and grasses, not only affects carbon sequestration through photosynthesis but also contributes to the carbon cycle as it decomposes and release carbon into atmosphere and soil. This process adds to soil organic matter and affects it carbon dynamics. Understanding the above and below-ground biomass of forest ground vegetation and its associated carbon pool is essential for improving local and glob
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Elliott, Jeannine, and Ronald Cook. "Design of Novel Corrosion Inhibiting Additives." In CORROSION 2008. NACE International, 2008. https://doi.org/10.5006/c2008-08213.

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Abstract While there is widespread use of organic molecules for prevention of corrosion in aqueous solution, their use in protective coatings has been restricted. Their effectiveness in protective coatings depends primarily on the carrier used to introduce the organic corrosion inhibitor into the coating, the molecular features of the corrosion inhibitor and the transport of the corrosion inhibitor to the active corrosion site. Organic corrosion inhibitors by themselves are difficult to incorporate into protective coatings due to differences in the specific gravities between the resins, other
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Pospelov, M., and A. Fokin. "Inhibition in Hydrocarbon and Hydrocarbon-Aqueous Media." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89137.

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Abstract Different proposed approaches to evaluating the mechanisms of corrosion inhibition of organic inhibitors of diphilic structure that contain both the polar and non-polar fragments are considered, special attention being paid to inhibition in media containing an aqueous electrolyte and a hydrocarbon phase. Critical analysis of the results of studies including those of the authors indicate that the broadly accepted conception of chemosorption and donor-acceptor bond on metal surfaces as the main factors responsible for the protective ability of an organic inhibitor cannot be applied to t
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Olivo, J. M. Domínguez, Shuyun Cao, D. Young, B. Brown, and S. Nesic. "Effect of Corrosion Inhibitor Head Group on the Electrochemical Processes Governing CO2 Corrosion." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14925.

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Abstract The use of corrosion inhibitors is a common practice used to mitigate internal pipeline corrosion in the oil and gas industry. An organic corrosion inhibitor is a molecule comprised of a head group (hydrophilic part) and an alkyl tail (hydrophobic part). Despite the significant amount of work associating the effect of the head group with the mode of adsorption of the inhibitor (such as bonding, effect on the tilt angle of the tail, and hysteresis), there is a lack of research relating the effect of the head group with the electrochemical processes governing the corrosion of mild steel
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Knudsen, Ole Øystein, Astrid Bjørgum, Tone Frydenberg, and Roy Johnsen. "Development of Internal Stress in Organic Coatings During Curing and Exposure." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06028.

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Abstract Internal stress in 21 different organic coatings has been measured by the beam deflection method. The internal stress was measured both after curing, after exposure in distilled water and after heating to 60°C. For most of the coatings investigated the measured internal stress was quite low and well below the level where cracking may become a problem. After exposure in distilled water the internal stress in most of the epoxy coatings increased significantly, but for most of the coatings the stress level was still quite low. For one of the epoxy coatings internal stress was calculated
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Natansohn, A., P. Rochon, J. Mao, and S. Xie. "Optical Storage in Polymers Containing Azo Groups without Electron-Donor - Electron Acceptor Substituents: Poly[4-(2-methacryloyloxy)ethyl-azobenzene]." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.25.

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Some degree of supramolecular organization can be induced in amorphous polymers containing azobenzene groups by means of polarized light. This phenomenon has been known for about a decade and the relevant literature has been reviewed in one of our recent publications1. This induced preferred orientation of the azobenzene groups can be monitored by a significant change in the refractive index of the polymer film and can thus be usea as an information storage mechanism. Circularly polarized light restores the natural disorder of the azobenzene orientations, enabling erasure of the stored informa
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Padmaperuma, Asanga B., and Carlos A. Fernandez. "Heteroleptic cyclometalated Ir(III) complexes with charge transporting groups: a theoretical study." In SPIE Organic Photonics + Electronics, edited by Franky So and Chihaya Adachi. SPIE, 2012. http://dx.doi.org/10.1117/12.949510.

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Berichte der Organisationen zum Thema "Organic groups"

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Knauss, K. G., and R. D. Aines. Experimental and theoretical modeling expertise of the Organic and Inorganic Environmental Geochemistry Groups. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/218213.

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Saveleva, Viktoria. The use of a phosphor in light sources in a photo cabinet. Light sources with a phosphor in a photo cabinet using laser diodes. Intellectual Archive, 2023. http://dx.doi.org/10.32370/iaj.2903.

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Non-thermal luminescence of a substance is called luminescence. This process occurs by absorbing excitation energy. The substance itself is called a phosphor. In chemical nature, the phosphor is divided into two groups: organic and non-organic. In fluorescent lamps and other light sources, a non-organic phosphor is used. The main purpose of using phosphor in lighting fixtures is to save energy. Another significant factor is the availability and low cost in the market. And also, the variety of colors available on the market. The use of phosphors with laser diodes is a new direction in lighting
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Kerakova, Maria, and Emilia Varadinova. Influence of the River Bottom Substrate and Sediment Organic Component on the Macrozoobenthos Functional Feeding Groups. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2020. http://dx.doi.org/10.7546/crabs.2020.01.08.

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DUDKINA, T. A. INCORPORATION OF ORGANIC MATTER INTO THE SOIL IN CROP ROTATIONS WITH DIFFERENT RATIOS OF CROP GROUPS. Ljournal, 2019. http://dx.doi.org/10.18411/issn1997-0749.2019-08-38-41.

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Santschi, Peter H. Complexation Reactions Between Trace Metals and Specific Functional Groups in Natural Organic Matter from Estuarine Waters. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada626695.

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Ganon, Rebecca, and Julie Kos. Student Disability Collectives in Australian Universities: A Desktop Review. Journal of the Australian and New Zealand Student Services Association, 2025. https://doi.org/10.30688/janzssa.2025-1-06.

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Student disability collectives (SDCs) are student-led groups which offer representation, social networks, and resources to university students with disability. They are run independently from the university administration. For the first time in published literature, this study has centralised and recorded information relating to the prevalence, nature, and function of SDCs. Desktop research targeting publicly available information about the prevalence, nature, and function of SDCs was undertaken to reveal a rich ecosystem of SDCs across up to 25 Australian universities. This study provides a f
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Clearfield, Abraham. Organic Derivatives of Layered Group (4) Phosphates. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada201080.

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Yates, Jr, and John T. Organic Functional Group Reactivities at Metal Surfaces. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada203094.

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Adam, Alexandre, Saadane Rezaiguia, Romain Severac, and Michel Bouquey. Incorporation of aminoalcohols to tune the properties of polyurethane systems. Universidad de los Andes, 2024. https://doi.org/10.51573/andes.pps39.gs.ps.1.

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It is common practice to incorporate low molecular weight molecules, known as chain extenders, to enhance the performance of polyurethane (PU) material. They usually increase the phase separation between the soft and hard domains, which has a significant impact on the density of hydrogen bonds. Aminoalcohols, molecules with both hydroxyl and amine functional groups, are important building blocks in the synthesis of pharmaceuticals but are also widely used in cosmetics or paints and coatings. Easily derived from abundant natural sources, such as amino acids, aminoalcohols align with the need fo
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Hoffman, F. Retardation of volatile organic compounds in ground water in low organic carbon sediments. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/39598.

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