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Relevant bibliographies by topics / Schiff Schiff

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Academic literature on the topic 'Schiff Schiff'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Schiff Schiff"

1

Çankaya, Nevin, Nevin Turan, and Özlem Sökmen. "SCHIFF BASE BIOPOLYMERS." e-Journal of New World Sciences Academy 1, no. 1 (September 10, 2016): 68–78. http://dx.doi.org/10.12739/nwsa.2016.1a11pb.

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Tülsner, Jens, and Ramona Herrfurth. "Schiff ahoi!" intensiv 26, no. 05 (September 2018): 228–30. http://dx.doi.org/10.1055/a-0641-9922.

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ZusammenfassungDie heutigen Einsatzmöglichkeiten von Fachkrankenpflegern sind breit. Verschiedene Disziplinen innerhalb und außerhalb des Krankenhauses sind dabei jedem bekannt, der sich gedanklich mit einer Veränderung seines beruflichen Umfelds beschäftigt. Mancher denkt auch über die Landesgrenzen hinaus, bezieht das nähere oder weitere Ausland in die Überlegungen für einen neuen Schritt mit ein. Dieser Artikel macht mit einem weiteren, weitgehend unbekannten Einsatzgebiet vertraut: Haben Sie schon einmal daran gedacht, auf einem Kreuzfahrtschiff zu arbeiten?

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Wiedemann, H. R. "Erwin Schiff." European Journal of Pediatrics 151, no. 12 (December 1992): 869. http://dx.doi.org/10.1007/bf01954119.

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Iacopetta, Domenico, Jessica Ceramella, Alessia Catalano, Carmela Saturnino, Maria Grazia Bonomo, Carlo Franchini, and Maria Stefania Sinicropi. "Schiff Bases: Interesting Scaffolds with Promising Antitumoral Properties." Applied Sciences 11, no. 4 (February 20, 2021): 1877. http://dx.doi.org/10.3390/app11041877.

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Schiff bases, named after Hugo Schiff, are highly reactive organic compounds broadly used as pigments and dyes, catalysts, intermediates in organic synthesis, and polymer stabilizers. Lots of Schiff bases are described in the literature for various biological activities, including antimalarial, antibacterial, antifungal, anti-inflammatory, and antiviral. Schiff bases are also known for their ability to form complexes with several metals. Very often, complexes of Schiff bases with metals and Schiff bases alone have demonstrated interesting antitumor activity. Given the innumerable vastness of data regarding antitumor activity of all these compounds, we focused our attention on mono- and bis-Schiff bases alone as antitumor agents. We will highlight the most significant examples of compounds belonging to this class reported in the literature.

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Wagh, Shaila, and B. R. Patil. "Synthesis and Spectral Characterization of Some New Novel Schiff bases Derived from Hydroxy Propiophenone." Oriental Journal Of Chemistry 37, no. 3 (June 30, 2021): 759–62. http://dx.doi.org/10.13005/ojc/370335.

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New Schiff bases derived by the condensation of methyl, chloro, and bromo substituted 2' hydroxy propiophenones with aliphatic and aromatic amines have been synthesized. The Schiff bases are yellow solids with sharp melting points. Schiff bases The spectral characterization of these newly synthesized Schiff base ligands has been done.These Schiff bases were characterized by IR spectroscopy, Nuclear magnetic resonance spectroscopy, UV spectroscopy, and Mass spectroscopy. IR spectra confirmed the presence of the phenolic OH group and azomethine group.

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Trofimova, Olga V., and Vladimir N. Trofimov. "ENTOMOPHAGES OF PINE CUTWORM (PANOLIS FLAMMEA SCHIFF.)." Bulletin of the Moscow State Regional University (Natural Sciences), no. 1 (2017): 39–48. http://dx.doi.org/10.18384/2310-7189-2017-1-39-48.

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Gangani, Bhavesh J., and Parsotam H. Parsania. "Conventional and Microwave Irradiated Syntheses of New Symmetric Double Schiff Bases of 1,1’-Bis(4-Amino Phenyl)Cyclohexane, their Spectral Characterization and Microbial Activity." International Letters of Chemistry, Physics and Astronomy 58 (September 2015): 33–39. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.58.33.

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Symmetric double Schiff bases of 1,1’- bis (4-amino phenyl) cyclohexane and substituted aromatic benzaldehydes were synthesized by thermal and microwave irradiated green chemistry techniques. The purity of Schiff bases was checked by TLC. The structure of Schiff bases were supported by UV, FTIR, 1HNMR and MS techniques. The antibacterial and antifungal activities of Schiff bases were checked against gram positive and gram negative microbes. Schiff bases showed moderate antibacterial activity but they showed good comparable antifungal activity against chosen microbes and standard drugs.

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Kajal, Anu, Suman Bala, Sunil Kamboj, Neha Sharma, and Vipin Saini. "Schiff Bases: A Versatile Pharmacophore." Journal of Catalysts 2013 (August 27, 2013): 1–14. http://dx.doi.org/10.1155/2013/893512.

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Schiff bases are condensation products of primary amines with carbonyl compounds gaining importance day by day in present scenario. Schiff bases are the compounds carrying imine or azomethine (–C=N–) functional group and are found to be a versatile pharmacophore for design and development of various bioactive lead compounds. Schiff bases exhibit useful biological activities such anti-inflammatory, analgesic, antimicrobial, anticonvulsant, antitubercular, anticancer, antioxidant, anthelmintic, antiglycation, and antidepressant activities. Schiff bases are also used as catalysts, pigments and dyes, intermediates in organic synthesis, polymer stabilizers, and corrosion inhibitors. The present review summarizes information on the diverse biological activities and also highlights the recently synthesized numerous Schiff bases as potential bioactive core.

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Celan, Paul. "Das Trunkene Schiff." Po&sie 124, no. 2 (2008): 25. http://dx.doi.org/10.3917/poesi.124.0025.

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Boden, Britta N., Amir Abdolmaleki, Cecily T. Z. Ma, and Mark J. MacLachlan. "New diformyldihydroxyaromatic precursors for luminescent Schiff base macrocycles: Synthesis, characterization, and condensation studies." Canadian Journal of Chemistry 86, no. 1 (January 1, 2008): 50–64. http://dx.doi.org/10.1139/v07-136.

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With the goal of preparing luminescent, fully conjugated Schiff base macrocycles, a series of precursors based on benzene, phenanthrene, and triphenylene with formylhydroxy functionalization have been prepared and characterized. The condensation of these compounds with substituted phenylenediamines to afford conjugated [2+2] or [3+3] Schiff base macrocycle has been investigated. Although the [3+3] Schiff base macrocycles could not be isolated, two new soluble and luminescent [2+2] Schiff base macrocycles with N2O2 binding pockets have been prepared and characterized.Key words: Schiff base, macrocycle, condensation, salicylaldehyde, conjugated.

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Dissertations / Theses on the topic "Schiff Schiff"

1

Chamayou, Anne-Christine [Verfasser], and Christoph [Akademischer Betreuer] Janiak. "Chiral metal-Schiff base complexes = Chirale Metal-Schiff-Base-Komplexe." Freiburg : Universität, 2011. http://d-nb.info/1115490567/34.

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Jensen, Svend Borup. "Schiff base calixarenes." Thesis, University of the West of Scotland, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246345.

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Four different synthetic routes to the sub-target, the p-tert-butylcalix[4lethylamine (6a) from thep-tert-butylcalix[4]arene (1a) have been examined. The best one was a 5-step synthesis, which gave an overall yield of65%. p-tert-Butylcalix[6]ethylamine (6b) and p-tert-butylcalix[8]ethylamine (6c) were synthesised from their respective p-tertbutylcalixarenes by the same route as the p-tert-butylcalix[4]ethylamine (6a). The three different amines (compound (6a), (6b) and (6c)) were used in 14 different Schiff -base type reactions which resulted in six Schiff-base compounds which were fully characterised by NMR, IR, FAB-ms and UV-vis. Insertion studies of the Schiff-base compounds along with template synthesis of the Schiff-base compounds were also attempted. The uptake of solid metal salt by the Schiff-base compounds in solution was examined by UV-vis spectroscopy. One of the Schiff -base compounds synthesised was the ferrocenecarboxaldehyde Schiff-base calix[4]arene (22a). An electrochemical analysis of this compound was undertaken to assess whether if it could be used as a sensor for metal ions. Molecular modelling of the Schiff-base compound and a crystal structure ofp-tert-butylcalix[4]ethylnitrile (8) are also presented in the thesis

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Boden, Britta Nicole. "Investigations of highly conjugated macrocycles and polymers for aggregation and chemical sensing." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/269.

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With the goal of developing Schiff base macrocycles with conjugation extended over multiple aromatic rings, new phenanthrene and triphenylene-containing bis(salicylates) were synthesized. A convenient route to 3,6,9,10-tetraalkoxy-2,7-diiodophenanthrene was developed. This compound has been found to be a useful precursor for Pd-catalyzed cross-coupling reactions. Macrocycles were synthesized by Schiff base condensation of the phenanthrene and triphenylene precursors. Reaction of smaller phenanthrene and triphenylene bis(salicylates) with 1,2-dialkoxy-4,5-phenylenediamine afforded macrocycles in poor yield and purity, but formation of the macrocycle was confirmed by mass spectrometry. Condensation of larger phenanthrene ethynylene bis(salicylates) with phenylenediamines formed [3+3] Schiff base macrocycles in good yield and could be purified through recrystallization. These two large macrocycles were weakly luminescent, and showed decrease in intensity of emission in solution over time. Addition of nitroaromatic compounds to solutions of the macrocycles caused quenching of luminescence, but Stern-Volmer constants could not be determined. One of the macrocycles aggregates in solution and shows some order in the solid state. Association constants for self-assembly of this macrocycle in chloroform were determined, and aggregation was found to be enthalpically driven and entropically disfavoured. Both large macrocycles can complex metals, but low solubility prevents thorough characterization of the metal complexes. Phenanthrene-containing poly(phenyleneethynylene)s (PPEs) and poly(phenylenevinylene)s (PPVs) were synthesized via the Sonogashira and Heckcouplings, respectively. The PPEs had high molecular weight and both polymers were extremely luminescent with OF = 70% for the PPE and OF = 59% for the PPV. These polymers show potential for use in solar cells and nitroaromatic sensors . Dithienylsalphen monomers were made using 4-(2-thienyl)salicylaldehyde and 5-(2-thienyl)salicylaldehyde. These monomers were coordinated to Ni(II), Cu(II) and vanadyl, and tested for electropolymerization. Conjugated dithienylsalphen monomers polymerize poorly, while non-conjugated dithienylsalphen monomers form good films through electropolymerization. Ultraviolet-visible spectroscopy confirmed extended conjugation in N,N '-phenylenebis(4-(2-thienyl)salicylideneimine).

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Leung, Alfred Chi Wook. "Conjugated schiff base-type metal-containing polymers." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/15889.

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The work in this thesis describes the synthesis and characterization of a series of conjugated polymers containing Schiff base transition metal complexes. High molecular weight poly(salphenyleneethynylene)s (PSPEs) were synthesized using the Sonogashira-Hagihara protocol and they were characterized using nuclear magnetic resonance spectroscopy and gel permeation chromatography. Their optical properties were investigated by UV-vis and fluorescence spectroscopies. PSPEs containing Zn saiphen moieties were found to exhibit strong aggregation that is facilitated by the presence of Zn to O interactions, and it was discovered that the polymers interact with various Lewis bases to undergo aggregation and deaggregation. New ladder-type conjugated polymers, as well as a series of model compounds that are representative of the repeating units of the polymers, were synthesized using Schiff base condensation methods. The electronic and magnetic properties of these ladder-polymers were studied using cyclic voltammetry, electron paramagnetic resonance spectroscopy, and magnetic susceptibility measurements.

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Wojciechowski, Paul E. "Electrochemistry of oxorhenium(V) Schiff base complexes." Thesis, Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/25988.

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Najera, Blanca A. "Schiff base macrocyclic ligands and their complexes." Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301827.

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Armstong, Douglas Charles. "Schiff base and related complexes of iron." Thesis, Imperial College London, 1985. http://hdl.handle.net/10044/1/37621.

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Ruwwe, Christian. "Volumetrische 3D-Modellierung aus unkalibrierten Freihandaufnahmen /." Tönning ; Lübeck Marburg : Der Andere Verl, 2008. http://d-nb.info/990884430/04.

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Provençal, Alexandre. "Synthetic strategies for self-assembled schiff-base macrocycles." Thesis, University of British Columbia, 2009. http://hdl.handle.net/2429/6048.

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Schiff-base macrocycles have interesting properties that could be used in new materials such as chemical sensors, catalysts and discotic liquid crystals. Triangular [3+3] Schiff-base macrocycles, for example, have been extensively studied in the MacLachlan group. However, few examples of [4+4] Schiff-base macrocycles have been reported. A square [4+4] Schiff-base macrocycle requires a precursor with the appropriate geometry such as compound 18. Synthesis of compound 18, however, proved to be problematic because of the formation of isomers, poor solubility and low yields. To avoid these issues, compound 36 was synthesized by Sonogashira coupling and was characterized by ¹H NMR spectroscopy, IR spectroscopy and HR-EI-MS. Reaction between compounds 36 and 37 led to the formation of an insoluble red solid. Although the characterization of this solid by NMR spectroscopy was not possible, MALDI-TOF data suggested that this solid contained the [4+4] Schiff-base macrocycle as the major product. A new synthetic approach to compound 11, widely used for the formation of [3+3] Schiff-base macrocycles, was devised. The overall yield is about 10% higher than the original synthesis of compound 11. Aside from the higher yield, this synthetic approach has other advantages over the previous one such as it does not require a large excess of reagents or expensive chemicals, all steps can be achieved on large scales and little purification between each step is required. All new intermediates were characterized by ¹H NMR spectroscopy, ¹³C NMR spectroscopy, IR spectroscopy and HR-EI-MS.

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Jiang, Jian. "Studies of supramolecular chemistry through Schiff-base chemistry." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/27809.

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This thesis describes the synthesis, characterization, and host-guest studies of a series of Schiff-base macrocycles. New [2+2] Schiff-base macrocycles were prepared by Schiff-base condensation. These macrocycles were shown to be wide-mouthed supramolecular hosts that can include organic cations such as pyridinium, paraquat and ammonium derivatives. A new kind of donor-acceptor-donor 3-in-1 complex was obtained in solution by combining macrocycle, cyclobis(paraquat-p-phenylene) and tetrathiafulvalene. Variations of these [2+2] Schiff-base macrocycles were prepared by modifying the substituents of the diformyl diol unit. In this way naphthalene-based macrocycles that undergo keto-enamine tautomerization were synthesized. These macrocycles can also combine with organic cations to form host-guest complex. The naphthalene-based [2+2] macrocycles can form lyotropic liquid crystals in chloroform and 1,2-dichloroethane. From the polarizing optical microscopy, it is proposed that the mesophases are lyotropic nematic liquid crystals based on a bilayer structure. A further study of these macrocycles shows that the host-guest complex can also form a lyotropic liquid crystalline phase. Covalently-linked macrocycles with isosceles triangle shapes were prepared by Schiff-base condensation. The molecular isosceles triangles proved to also be supramolecular hosts for pyridinium and ammonium cations, based on ¹H NMR, 2D-ROESY NMR, and mass spectrometry studies. In addition to the Schiff-base macrocycles, conjugated Schiff-base containing oligomers were synthesized via Gilch polymerization methods. The oligomers were characterized by gel permeation chromatography (GPC), thermogravimetric analysis (TGA) and UV-Vis spectroscopy. For further proof of the oligomeric structure, a model compound was prepared by the Wittig reaction.

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Books on the topic "Schiff Schiff"

1

Storz, Claudia. Das Schiff. Zurich: Nagel & Kimche, 1989.

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Leutenegger, Gertrud. Komm ins Schiff. Frankfurt am Main: Suhrkamp Taschenbuch Verlag, 1989.

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Storz, Claudia. Das Schiff: Roman. Zürich: Nagel & Kimche, 1989.

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Klinger, Kurt. Das blühende Schiff. Wien: Der Apfel, 1998.

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Konsalik, Heinz G. Schiff der hoffnung. München: Wilhelm Heyne Verlag, 1989.

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Mand, Andreas. Das rote Schiff: Roman. Augsburg: MaroVerlag, 1994.

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Bresciani, Edda. La Collezione Schiff Giorgini. Pisa: Giardini, 1992.

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Das rote Schiff: Roman. Käsmayr: Maroverlag, 1994.

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Precht, Georg Jonathan. Das Schiff im Noor: Roman. München: Limes, 1999.

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Das Schiff der hansischen Frühzeit. 2nd ed. Weimar: H. Böhlaus Nachfolger, 1986.

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Book chapters on the topic "Schiff Schiff"

1

Pompl, Wilhelm. "Schiff." In Springer-Lehrbuch, 287–304. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59147-1_8.

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Pompl, Wilhelm. "Schiff." In Springer-Lehrbuch, 258–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-97558-5_8.

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Classen, Alexander. "Hafen, Schiff." In Literarische Orte in deutschsprachigen Erzählungen des Mittelalters, edited by Tilo Renz, Monika Hanauska, and Mathias Herweg, 241–49. Berlin, Boston: De Gruyter, 2018. http://dx.doi.org/10.1515/9783050093918-016.

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Gooch, Jan W. "Schiff Base." In Encyclopedic Dictionary of Polymers, 647. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10332.

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Scarpa, Carlo. "Insel und Schiff." In Die Unterseite der Architektur, 170–83. Vienna: Springer Vienna, 2008. http://dx.doi.org/10.1007/978-3-211-78654-3_20.

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Dupré, Ben. "Das Schiff des Theseus." In 50 Schlüsselideen Philosophie, 40–43. Heidelberg: Spektrum Akademischer Verlag, 2010. http://dx.doi.org/10.1007/978-3-8274-2395-5_11.

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Boucher, L. J., Karl Koeber, Dieter Tille, Helga Demmer, Helga Köttelwesch, and Edith Schleitzer-Rust. "Complexes with Schiff Bases." In Mn Manganese, 3–238. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-662-08178-5_2.

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Li, Jia, and René C. Steininger. "Fahrzeug und Schiff steuer (VVT)." In Steuerstandort China, 200–203. Wiesbaden: Gabler, 2010. http://dx.doi.org/10.1007/978-3-8349-8521-7_19.

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Gower, Adam. "Jacob Schiff and His Cohort." In Jacob Schiff and the Art of Risk, 75–107. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-90266-1_3.

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Fortmann-Hijazi, Sarah. "Fatah, Sherko: Das dunkle Schiff." In Kindlers Literatur Lexikon (KLL), 1–2. Stuttgart: J.B. Metzler, 2020. http://dx.doi.org/10.1007/978-3-476-05728-0_1628-1.

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Conference papers on the topic "Schiff Schiff"

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ENGEL, J. "SCHIFF MOMENTS AND NUCLEAR STRUCTURE." In Proceedings of the Fourth Argonne/INT/MSU/JINA FRIB Theory Workshop. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789814271738_0004.

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"Biological Applications of Tryptamine Schiff Base Derivatives." In Nov. 27-28, 2017 South Africa. EARES, 2017. http://dx.doi.org/10.17758/eares.eap1117040.

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"Biological Applications of Tryptamine Schiff Base Derivatives." In Nov. 27-28, 2017 South Africa. EARES, 2017. http://dx.doi.org/10.17758/eares.eap517210.

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Mazurak, Zbigniew, K. Gornik, and D. Sek. "Fluorescence properties of the Schiff-base polymers." In 2000 International Conference on Application of Photonic Technology (ICAPT 2000), edited by Roger A. Lessard and George A. Lampropoulos. SPIE, 2000. http://dx.doi.org/10.1117/12.406464.

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Geethalakshmi, V., N. Nalini, and C. Theivarasu. "Anticancer activity of morpholine schiff base complexes." In PROCEEDINGS OF ADVANCED MATERIAL, ENGINEERING & TECHNOLOGY. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0024590.

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Yoshinaga, Naotaka, Eri Teruya, Koji Higashiyama, and Kota Yanase. "Nuclear Schiff Moments in Medium and Heavy Nuclei." In Proceedings of the Ito International Research Center Symposium "Perspectives of the Physics of Nuclear Structure". Journal of the Physical Society of Japan, 2018. http://dx.doi.org/10.7566/jpscp.23.012034.

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Fondo, Matilde, Cristina Portela-Garcia, Jesus Sanmartín-Matalobos, and Ana García-Deibe. "Schiff base hydrolysis mediated by d-block metals." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a026.

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Sharma, Ranjana, Y. C. Goswami, Rajeev Singh, and D. Kumar. "Synthesis of CdS nanostructures using Schiff base complexes." In Proceedings of the International Conference on Nanotechnology for Better Living. Singapore: Research Publishing Services, 2016. http://dx.doi.org/10.3850/978-981-09-7519-7nbl16-rps-212.

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PEROBELLI, Giullia, Nayara G. S. CAVALCANTE, Ana Cristina F. de Brito PONTES, and Daniel de Lima PONTES. "Esferas de quitosana: produção de bases de schiff." In 5º Encontro Regional de Química & 4º Encontro Nacional de Química. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/chenpro-5erq-in2.

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Fondo, Matilde, Jesús Sanmartín, Noelia Ocampo, and Ana García-Deibe. "Double imidazolidine condensation in a polynucleating Schiff base." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00425.

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Reports on the topic "Schiff Schiff"

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Zauche, Timothy. Kinetics and mechanisms of the oxidation of alcohols and hydroxylamines by hydrogen peroxide, catalyzed by methyltrioxorhenium, MTO, and the oxygen binding properties of cobalt Schiff base complexes. Office of Scientific and Technical Information (OSTI), February 1999. http://dx.doi.org/10.2172/770652.

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Pieper, S. C., and R. B. Wiringa. Nolen-Schiffer anomaly. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/166459.

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Verdonschot, Piet F. M., and Dorine T. B. M. Dekker. Stekende insecten Borkel & Schaft : verkenning 2017. Wageningen: Zoetwaterecosystemen, Wageningen Environmental Research, 2017. http://dx.doi.org/10.18174/440222.

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Research Institute (IFPRI), International Food Policy. Welthunger-Index 2017: Wie Ungleichheit Hunger schafft. Washington, DC: International Food Policy Research Institute, 2017. http://dx.doi.org/10.2499/9780896292727.

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Campbell, J. E., and P. J. Henderson. Surficial geology, Denare Beach-Schist Lake, Saskatchewan-Manitoba. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1997. http://dx.doi.org/10.4095/209396.

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Research Institute (IFPRI), International Food Policy. Welthunger-Index 2017: Wie Ungleichheit Hunger schafft: Synopse. Washington, DC: International Food Policy Research Institute, 2017. http://dx.doi.org/10.2499/9780896292765.

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Erdmer, P. The Nisling Schist in eastern Dezadeash map area, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1989. http://dx.doi.org/10.4095/127470.

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Buchmueller, Thomas, Anthony Lo Sasso, and Kathleen Wong. How Did SCHIP Affect the Insurance Coverage of Immigrant Children? Cambridge, MA: National Bureau of Economic Research, July 2007. http://dx.doi.org/10.3386/w13261.

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Digel, S., and T. M. Gordon. Low - To Medium - Grade Metamorphism of Metabasites At Schist Lake, near Flin Flon, Manitoba. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1990. http://dx.doi.org/10.4095/131243.

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Hannibal, Joseph T. Bringing millstones to America: 19th century use of Norwgian mica-schist millstones in the United States. Universitat de Lleida. Departament d'Història. Secció d'Arqueologia, Prehistòria i Història Antiga, 2019. http://dx.doi.org/10.21001/rap.2019.extra-4.21.

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