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Relevant bibliographies by topics / Molecular compounds of thiocarbamides

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Academic literature on the topic 'Molecular compounds of thiocarbamides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Molecular compounds of thiocarbamides"

1

Kul'kov, M. G., G. T. Salakhidinova, E. A. Vtorushina, R. I. Butyrin, and A. E. Aliev. "Quantification of C10–C14 Adamantanes in High-Viscosity Naphthenic Oils." Нефтехимия 63, no. 5 (2023): 654–70. http://dx.doi.org/10.31857/s0028242123050039.

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The paraffin–naphthenic fractions (with boiling points below 310°C) prepared from three high-viscosity naphthenic crude oils, classified as types B1 and B2 (according to Petrov’s classification), were subjected to thiocarbamide complexation. The molecular composition of polycyclic hydrocarbon biomarkers and C11–C13 adamantanes in the oil samples suggested a predominantly marine genotype of the precursor organic matter (OM). The molecular composition also suggested source rocks of a clayey type. Nonetheless, the biomarkers detected in one sample indicated some contribution of terrigenous compon

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Sermakasheva, N. L., G. F. Novikov, Yu M. Shul'ga, and V. N. Semenov. "Microwave photoconductivity and photodielectric effect in thin PbS films obtained from thiocarbamide coordination compounds." Semiconductors 38, no. 4 (2004): 380–86. http://dx.doi.org/10.1134/1.1734662.

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Prashant, R. Mahalle, V. Korpe Gajanan, and P. Deshmukh Shirish. "New N-galactosides : Synthesis of N-galactosylated thiocarbamides, benzothiazolyl thiocarbamides and thiocarbamates." Journal of Indian Chemical Society Vol. 85, Sep 2008 (2008): 953–58. https://doi.org/10.5281/zenodo.5820384.

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P.G Department ofChemisty, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail:</em> prmahalle@rediffmail.com <em>Manuscript received 22 August 2007, revised 22 May 2008, accepted 3 June 2008</em> The title compounds were prepared by the condensation of tetra-<em>O</em>-acetyi-β-D-galactopyranosyl isothiocyanate with several amines, 2-aminobenzothiazole/substituted benzothiazoles and alcohols respectively. The structure of these new <em>N</em>-galactoside has been established on the basis of usual chemical transformations and IR, NMR and Mass spectral studies of some typica

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Pawar, Swati. "Synthesis and Antithyroidal Evaluation of N–Aryl Formamidino–N–(Substituted) Aryl Thiocarbamides." International Journal of Advance Research and Innovation 2, no. 1 (2014): 25–35. http://dx.doi.org/10.51976/ijari.211404.

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Several N–aryl formamidino derivatives of thiocarbamides were synthesized. The structure and purity of the prepared compounds were characterized by elemental, spectral (IR) and TLC analysis. These molecules were evaluated for their efficacy as antithyroidals by radioactive iodine uptake method the activity (Potency) of synthesized compounds were compared with standard drug Thiouracil.

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Wang, Yuan-Peng, Ting-Ting Jiang, Jie Sun, et al. "Synthesis, structure, theoretical calculation and antibacterial property of two novel Zn(II)/Ni(II) compounds based on 3, 5-dichlorosalicylaldehyde thiocarbamide ligand." Bioorganic Chemistry 144 (March 2024): 107140. http://dx.doi.org/10.1016/j.bioorg.2024.107140.

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S., K. Deshmukh, T. Agrawal P., and P. Deshmukh S. "Synthesis and antimicrobial activity of some new lactosylated-1 ,2,4-dithiazolidine (hydrochlorides)." Journal of Indian Chemical Society Vol. 88, Nov 2011 (2011): 1759–62. https://doi.org/10.5281/zenodo.5791770.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India P. G. Department of Chemistry, Shri R. L. T. College of Science, Akola, Maharashtra, India <em>Manuscript received 06 October 2009, revised 23 February 2011, accepted 25 April 2011</em> Several 3-hepta-0-benzoyl-P-n-lactosylimino-4-aryl-5-phenylimino and 4-phenyl-5-hepta-0-acetyi-P-DIactosylimino-3-arylimino-1,2,4-dithiazolidine (hydrochlorides) have been prepared by the interaction of 1-hepta-0-benzoyi-β-D-lactosyl-3-aryl thiocarbamides and <em>N</em>-phenyl-<em>S</em>-chloro isothiocarbamoyl chloride a

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Маскаева, Л. Н., Е. В. Мостовщикова, В. Ф. Марков та В. И. Воронин. "Структурные, оптические и фоточувствительные свойства пленок PbS, осажденных в присутствии CaCl-=SUB=-2-=/SUB=-". Физика и техника полупроводников 53, № 2 (2019): 174. http://dx.doi.org/10.21883/ftp.2019.02.47095.8907.

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AbstractPolycrystalline lead-sulfide (PbS) films doped with calcium are synthesized on sitall and glass substrates by chemical bath deposition with the use of thiocarbamide and a CaCl_2 additive at concentrations of up to 5 mM. Introduction of the CaCl_2 additive into the reaction solution greatly prolongs the induction period of the process of synthesis. The thicknesses of the PbS and PbS(Ca) films are, correspondingly, 200 and 150 nm at an average crystallite dimension of ~100 nm. The maximum calcium content in the films is 0.06 at % for layers on sitall substrates and 0.11 at % for layers o

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S., P. DESHMUKH, and G. PARANJPE M. "Synthesis of N-Glucopyranosyl Benzothiazolyl Thiocarbamides." Journal of Indian Chemical Society Vol. 62, May 1985 (1985): 375–76. https://doi.org/10.5281/zenodo.6302905.

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Department of Chemistry, Nagpur University, Nagpur-440 010 <em>Manuscript received 18 September 1984, revised 5 February 1985, accepted 29 April 1985</em> 1-Tetra-<em>O</em>-acetyl-<em>β</em>-D-glucopyranosyl-3-substituted-benzothiazolyl thiocarbamides (3) have been prepared by the interaction of tetra-<em>O</em>-acetyl-<em>β</em>-D-glueopyranosyl isothiocyanate and 2-aminobenzothiazole/substituted-benzothiazoles.

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M., Zahurul Haque, Omar Faruq M., and Umar Ali M. "Synthesis of some new thiocarbamides from a constituent of lac and studies on their antimicrobial activities." Journal of Indian Chemical Society Vol. 79, Oct 2002 (2002): 841–42. https://doi.org/10.5281/zenodo.5847960.

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BCSIR Laboratories, Rajshahi, Bangladesh <em>E-mail : </em>bcsirraj @librabd.net Department of Chemistry, Rajshahi University, Rajshahi, Bangladesh <em>Manuscript received 21 May 2001, revised 14 February 2002, accepted 24 April 2002</em> Some new thiocarbamides have been synthesized by the reaction of aleurityl hydrazide (prepared from aleuritic acid isolated from Bangladeshi lac) with different isothiocyanates. Antibacterial activities of the compounds have been determined and most of them are found highly active.

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Samidha, S. Kadu, V. Korpe Gajanan, and P. Karyakarte R. "Novel synthesis of some N-glycosyl benzimidazolyl thiocarbamides and their antimicrobial activity." Journal of Indian Chemical Society Vol. 93, Dec 2016 (2016): 1389–92. https://doi.org/10.5281/zenodo.5598963.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : samidhakadu@gmail.com Department of Microbiology, Govt. Medical College, Akola-444 001, Maharashtra, India <em>Manuscript received online 25 July 2015, accepted 09 August 2016</em> Several 1-peracetyl and perbenzoyl glycosyl benzimidazolyl thiocarbamides were synthesized by the interaction of peracetyl and perbenzoyl glycosyl isothiocyanate and 2-amino benzimidazole. The identities of these newly synthesized compounds were established on the basis of usual chemical transformations and IR, <s

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Dissertations / Theses on the topic "Molecular compounds of thiocarbamides"

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Grant, Guy Hamilton. "Molecular modelling of silicon compounds." Thesis, University of Liverpool, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329403.

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Gracin, Sandra. "Solubility and polymorphism of molecular compounds /." Stockholm, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-267.

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Beck, Elizabeth Rose. "Molecular recognition by novel macrocyclic compounds." Thesis, University of Hull, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337244.

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Stead, William John. "Neutron scattering from molecular metallic compounds." Thesis, University of Oxford, 1986. http://ora.ox.ac.uk/objects/uuid:a1978bc4-b4ff-42c4-855a-7103b39a75c1.

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The alkali metal graphite intercalates and the conducting polymers polyacetylene and polypyrrole are reviewed and compared. Polyacetylene was synthesized by Luttinger's method and doped by exposure to caesium vapour. The doped and undoped polyacetylene were characterized by neutron powder diffraction. Hydrogen absorption and subsequent pyrolysis of caesium doped polyacetylene were studied. Mass spectrum analysis of the gases evolved at 300°C showed methane and other alkanes, indicating H<sub>2</sub> addition to the polymer chain followed by methane elimination. The graphite intercalates C<sub>

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Brookman, Charles Alexander. "The molecular structures of some heterocyclic compounds." Thesis, University of Edinburgh, 1993. http://hdl.handle.net/1842/12791.

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The gas-phase molecular structures of 2-chloropyridine, 3-chloropyridine, 4-chloropyridine, chloropyrazine, 1,2,3-triazine, 1,3,5-triazine and 1,2,4,5-tetrazine have been determined by electron differaction, and, in the case of the first two and the fourth, by combining them with microwave spectoscopy data. Of particular interest was the combination of ring distortion effects arising from both the chlorine substituent and the nitrogen heteratom. The results tend to indicate a more complicated system than that of purely substituent effects, an area already well documented. One of the interestin

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Tuncel, van Pomeren Binnur. "Molecular complexes of 4,4'-dinitrobiphenyl." Pretoria : [s.n.], 2004. http://upetd.up.ac.za/thesis/available/etd-03132006-155913.

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Yu, Pui-yin. "Metal alkylidyne complexes as building blocks for molecular materials /." Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19470514.

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O'Neill, Andrew. "Investigations in molecular structure : from scattering to molecular complexes of brominated compounds." Thesis, University of Glasgow, 2010. http://theses.gla.ac.uk/1709/.

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The main focuses of this research were to examine the capabilities of solution techniques to attempt to monitor the nucleation process in crystallisation, and to investigate structural outcomes of crystallisation processes, with reference to polymorphism and intermolecular interactions. To achieve this, work on the investigation of nucleation and early-stage crystallisation was carried out at the Department of Pharmaceutical Sciences at the University of Strathclyde and also at the central synchrotron facility of Station 2.1 at the SRS Daresbury. Small angle X-ray scattering (SAXS) was carried

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Kueh, Alona Swee Hua. "Molecular imprinting of small, poorly functionalised organic compounds." The University of Waikato, 2008. http://hdl.handle.net/10289/2264.

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Molecularly imprinted polymers (MIPs) have been compared to natural antibodies in that they can specifically bind target compounds in a similar way that antibodies specifically bind to an antigen. The attraction of the MIPs technology is the ease of creating binding elements which are relatively cheap compared with the process of isolating natural antibodies. In this research monoterpenes, such as α-terpineol, were chosen to be the model compounds for investigating the molecular imprinting of small, poorly functionalised organic compounds. The conventional non-covalent approach was mainly u

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Scouter, Philip F. "Molecular compounds of the heavier Group 13 elements." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308610.

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Books on the topic "Molecular compounds of thiocarbamides"

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Minkin, V. I., L. P. Olekhnovich, and Yu A. Zhdanov, eds. Molecular Design of Tautomeric Compounds. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1429-2.

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Scheschkewitz, David, ed. Functional Molecular Silicon Compounds I. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03620-5.

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Scheschkewitz, David, ed. Functional Molecular Silicon Compounds II. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03734-9.

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Petrovich, Olekhnovich Lev, and Zhdanov I͡U︡ A, eds. Molecular design of tautomeric compounds. D. Reidel Pub. Co., 1988.

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I͡A, Lukevit͡s Ė. Molecular structure of organosilicon compounds. E. Horwood, 1989.

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6

Comba, Peter. Molecular modeling of inorganic compounds. 2nd ed. Wiley-VCH, 2001.

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Comba, P. Molecular modeling of inorganic compounds. VCH, 1995.

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W, Hambley Trevor, and Martin Bodo, eds. Molecular modeling of inorganic compounds. 3rd ed. Wiley-VCH, 2009.

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Comba, Peter. Molecular modeling. VCH, 1995.

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E, Weber, and Gerdil R, eds. Molecular inclusion and molecular recognition: Clathrates I. Springer-Verlag, 1987.

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Book chapters on the topic "Molecular compounds of thiocarbamides"

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Lerf, A. "Molecular Intercalation Compounds." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145203.ch172.

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Furka, Árpád. "Organonitrogen Compounds." In SpringerBriefs in Molecular Science. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06004-6_4.

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Furka, Árpád. "Organosulfur Compounds." In SpringerBriefs in Molecular Science. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06004-6_5.

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Furka, Árpád. "Inorganic Compounds." In SpringerBriefs in Molecular Science. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06004-6_8.

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Yokoyama, Yasushi, Tsuyoshi Gushiken, and Takashi Ubukata. "Fulgides and Related Compounds." In Molecular Switches. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634408.ch3.

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Vančik, Hrvoj. "Molecular Structures." In Aromatic C-nitroso Compounds. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6337-1_1.

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Delaigue, Xavier, Ernest Graf, Frédérique Hajek, Mir Wais Hosseini, and Jean Marc Planeix. "Molecular Tectonics." In Crystallography of Supramolecular Compounds. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-1692-0_10.

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Jongh, L. J., and J. Sinzig. "Metal Cluster Compounds." In Molecular Magnetism: From Molecular Assemblies to the Devices. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-017-2319-0_12.

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Zhang, Yifeng, Meirong Jia, and Wei Gao. "Synthetic Biology of Active Compounds." In Molecular Pharmacognosy. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-32-9034-1_9.

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Das, Bhaskar C., Devi Prasan Ojha, Sasmita Das, and Todd Evans. "Boron Compounds in Molecular Imaging." In Boron-Based Compounds. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119275602.ch2.4.

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Conference papers on the topic "Molecular compounds of thiocarbamides"

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Biswas, Aritra, Pablo Cencillo-Abad, and Debashis Chanda. "Probing Molecular Chirality with a Tunable Achiral Plasmonic System." In CLEO: Fundamental Science. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_fs.2024.ff3c.5.

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We demonstrate helicity preserving engineered chiral light on a tunable achiral nanostructured SEIRA-VCD platform that can enable precise detection and classification of diverse chiral compounds, reshaping drug design and biomolecular applications.

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Jursenas, S., A. Groudis, G. Kodis, and L. VaIkunas. "Spectroscopy of Polar Molecular Compounds." In EQEC'96. 1996 European Quantum Electronic Conference. IEEE, 1996. http://dx.doi.org/10.1109/eqec.1996.561918.

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Medcraft, Chris, Melanie Schnell, Simon Merz, David Schmitz, V. Shubert, and Thomas Betz. "CHARACTERISATION AND CONTROL OF COLD CHIRAL COMPOUNDS." In 69th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.tb01.

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Cappelluti, E. "Nonadiabatic channels in fullerene compounds." In ELECTRONIC PROPERTIES OF MOLECULAR NANOSTRUCTURES: XV International Winterschool/Euroconference. AIP, 2001. http://dx.doi.org/10.1063/1.1426828.

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Souza, Gabriel L. C. de, Shawan K. C. Almeida, and Rodrigo A. Mendes. "Antioxidant activity of myricetin-like compounds." In VII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Editora Letra1, 2018. http://dx.doi.org/10.21826/9788563800374002.

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Descamps, M. "Non Equilibrium Transformations of Molecular Compounds Induced Mechanically." In FLOW DYNAMICS: The Second International Conference on Flow Dynamics. AIP, 2006. http://dx.doi.org/10.1063/1.2204463.

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Zhu, Cheng, Leonid Khriachtchev, and Markku Räsänen. "INFRARED MATRIX-ISOLATION STUDY OF NEW NOBLE-GAS COMPOUNDS." In 71st International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.mk06.

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Takenobu, T. "Synthesis of organics/SWNT compounds." In MOLECULAR NANOSTRUCTURES: XVII International Winterschool Euroconference on Electronic Properties of Novel Materials. AIP, 2003. http://dx.doi.org/10.1063/1.1627990.

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Duchko, Maria, Irina Russkikh, Evgeniya Strelnikova, Lidiya Svarovskaya, and Olga Serebrennikova. "INFLUENCE OF BIODEGRADATION ON THE ORGANIC COMPOUNDS COMPOSITION OF PEAT." In 71st International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.wk12.

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Porterfield, Jessie, Barney Ellison, John Daily, et al. "THERMAL DECOMPOSITION OF THE LIGNIN MODEL COMPOUNDS: SALICYLALDEHYDE AND CATECHOL." In 73rd International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.mj10.

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Reports on the topic "Molecular compounds of thiocarbamides"

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Kokpol, Sirirat. Relationships between biological activity and molecular properties of artemisinin compounds. Chulalongkorn University, 2001. https://doi.org/10.58837/chula.res.2001.38.

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Relationships between biological activity and molecular properties of 68 antimalarial artemisinin compounds were investigated in the quantitative manner. All compounds were geometrically optimized at the HF/3-21G level. Totally 102 molecular properties covering hydrophobicity, polarizability, electronic, and steric parameters were calculated from the optimized structures. The activities against 2 different strains of malarial parasites, D-6 and W-2, were taken from the literatures. Statistical analyses were performed to find the relationships between the activities and the calculated molecular

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Midey, Anthony. Ion-Molecular Reactions With Organic and Atmospheric Compounds from 150-1400K. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada405891.

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Suria, Sabartanty. Intermolecula transfer and elimination of molecular hydrogen in thermal reactions of unsaturated organic compounds. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/108159.

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Venkat, Rama. DEPSCOR Molecular Beam Epitaxy of Low Temperature Non-Stoichiometric III-V Compounds: Theoretical Modeling and Simulation. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada368284.

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Kotwal, Shashikant. Grant: Automation of BitterX Molecular Docking of Bitter taste compounds to Human Bitter Taste Receptors (TAS2R). ResearchHub Technologies, Inc., 2025. https://doi.org/10.55277/researchhub.b0nzqfac.

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Rocheford, Torbert, Yaakov Tadmor, Robert Lambert, and Nurit Katzir. Molecular Marker Mapping of Genes Enhancing Tocol and Carotenoid Composition of Maize Grain. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7571352.bard.

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The overall objective of this research was to identify chromosomal regions and candidate genes associated with control of concentration and forms of carotenoids (includes pro-Vitamin A) and tocopherols (Vitamin E), which are both antioxidants and are associated with health advantages. Vitamin A and E are included in animal feeding supplements and the eventual goal is to increase levels of these compounds in maize grain so that the cost of these supplements can be reduced or eliminated. Moreover, both compounds are antioxidants that protect unsaturated fatty acids from oxidation and thus mainta

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Brel, Valery K. Development of the New Approaches in Designing of Fluoroorganic Derivatives Sulfur (Unsaturated, Heterocyclic, Aromatic Molecular Systems and Polyfunctional Organic Compounds). Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada447113.

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Schutt, Timothy C., and Manoj K. Shukla. Computational Investigation on Interactions Between Some Munitions Compounds and Humic Substances. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/39703.

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Humic acid substances (HAs) in natural soil and sediment environments effect the retention and degradation of insensitive munitions compounds and legacy high explosives (MCs): DNAN, DNi- NH4+, nMNA, NQ, NTO (neutral and anionic forms), TNT, and RDX.A humic acid model compound has been considered using molecular dynamics, thermodynamic integration, and density functional theory to characterize the munition binding ability, ionization potential, and electron affinity compared to that in the water solution. Humic acids bind most compounds and act as both a sink and source for electrons. Ionizatio

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Rafaeli, Ada, and Russell Jurenka. Molecular Characterization of PBAN G-protein Coupled Receptors in Moth Pest Species: Design of Antagonists. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7593390.bard.

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The proposed research was directed at determining the activation/binding domains and gene regulation of the PBAN-R’s thereby providing information for the design and screening of potential PBAN-R-blockers and to indicate possible ways of preventing the process from proceeding to its completion. Our specific aims included: (1) The identification of the PBAN-R binding domain by a combination of: (a) in silico modeling studies for identifying specific amino-acid side chains that are likely to be involved in binding PBAN with the receptor and; (b) bioassays to verify the modeling studies using mut

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Chefetz, Benny, and Jon Chorover. Sorption and Mobility of Pharmaceutical Compounds in Soils Irrigated with Treated Wastewater. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7592117.bard.

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Research into the fate of pharmaceutical compounds (PCs) in the environment has focused on aspects of removal efficiency during sewage treatment, degradation in surface water and accumulation in soils and sediments. However, very little information is available on the binding interactions of pharmaceuticals with dissolved organic matter (DOM) originating from wastewater treatment. Such interactions can significantly affect the transport potential of PCs in soils by altering compound affinity for soil particle surfaces. Our primary hypothesis is that the transport potential of PCs in soils is s

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