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Journal articles on the topic 'Molecular compounds of thiocarbamides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Talekar, P. R. "Effects on Germination Pattern of Jowar of Novel Synthesis of N-Substituted thioamidodicyandiamide." International Journal of Advance and Applied Research 5, no. 23 (2024): 121–26. https://doi.org/10.5281/zenodo.13621901.

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Abstract:  Plant physiology has increasingly important role in agricultural research problem. One of the primary tasks in the future will be to increase production of food and resist pathogen of the crop. Organic drugs have intense biological activity to the seed before sowing in order to control and suppress the pathogens. So the aim of the present work is to study the above said topic. In the present work in our laboratory novel series of 1-[S-TAG-N substituted thioamido] dicyandiamide have been synthesized successfully by refluxing TAG Br with cyanoamidino substituted thiocarbamid

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12

Siddharth. A. Waghmare and Kuldip U. Dongare. "Design, synthesis, and spectral characterization of series of thiocarbamides with coumarin backbone." International Journal of Science and Research Archive 10, no. 2 (2023): 855–59. http://dx.doi.org/10.30574/ijsra.2023.10.2.1035.

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Recently a series of 7-(3-thiocarbamido), 7-(3-phenylthiocarbamido), 7-(3-(1,3-dimethyl) thiocarbamido), 7-(3-methylthiocarbamido), 7-(3-allylthiocarbamido)-4-methyl-2H-chromen-2-one (IIIa-e) had been synthesized by refluxing 7-chloro-4-methyl-2H-chromen-2-one (I) with thiourea, N-phenylthiourea, 1,3-dimethylthiourea, N-methylthiourea and N-allylthiourea (IIa-e) in isopropanol medium in 1:1 molar proportion for 5 hours. All the synthesized compounds structures were justified on the basis of chemical tests, elemental study and spectral characterization.

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13

Pradip, P. Deohate, and N. Berad B. "The convenient microwave-assisted synthesis, characterization and structural study of substituted bis-[1,2,4]-dithiazolidines." Journal of Indian Chemical Society Vol. 91, Jul 2014 (2014): 1361–64. https://doi.org/10.5281/zenodo.5726594.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India Department of Chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440 033, Maharashtra, India <em>E-mail </em>: pradip222091@yahoo.co.in <em>Manuscript received online 05 December 2012, revised 21 February 2014, accepted 28 February 2014</em> A convenient synthesis of substituted bis-[1,2,4]-dithiazolidines has been developed by using the environmentfriendly technique of microwave irradiation. The microwave-assisted synthesis of several members of the titled class

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14

P. L. Harale, M. E. Shelke, D.T. Tayade, and A. R. Kurhe. "Synthesis of 3-(substitutedthiocarbamide)-aniline derivatives from di-tert-butyl dicarbonate (BoC) protected 3-chloroaniline." GSC Biological and Pharmaceutical Sciences 28, no. 3 (2024): 046–52. http://dx.doi.org/10.30574/gscbps.2024.28.3.0313.

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Synthesis of substituted thiocarbamide derivatives is important in the fields of medicinal, agricultural, chemical, and pharmaceutical. Thiocarbamides are commonly utilized as starting materials for several organic synthetic processes and have been studied in search for easy and effective methods of chemical synthesis. In the existing research work, 3-chloroaniline was protected by a di-tert-butyl dicarbonate (BoC) protecting agent. Substituted thiocarbamide derivatives were synthesized using condensation of various substituted thioureas with amino group-protected 3-chloroaniline. The structur

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15

Mopari, Anuja M., and Gajanan V. Korpe. "Synthesis and Structural Studies of N-Maltosylated Aryl Thiobiurets." Asian Journal of Chemistry 34, no. 5 (2022): 1220–24. http://dx.doi.org/10.14233/ajchem.2022.23649.

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The derivatives of urea, thiourea and thiosemicarbazide play an important role in medicinal chemistry by influencing various pharmacological activities. The design and development of novel N-maltosides have emerged as an important class of organic compounds. A series of 1-hepta-O-benzoyl-β-D-Maltosyl- 5-aryl-2-4-thiobiurets are described in present work. By mixing hepta-O-benzoyl→D-maltosyl isocyanates with various aryl thiocarbamides, 1-hepta-O-benzoyl-β-D-maltosyl-5-aryl-2-4-thiobiurets have been synthesized. The identities of this newly synthesized 1-hepta-O-benzoyl-β-D-Maltosyl-5- aryl-2-4

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16

P., L. Harale, E. Shelke M., Tayade D.T., and R. Kurhe A. "Synthesis of 3-(substitutedthiocarbamide)-aniline derivatives from di-tert-butyl dicarbonate (BoC) protected 3-chloroaniline." GSC Biological and Pharmaceutical Sciences 28, no. 3 (2024): 046–52. https://doi.org/10.5281/zenodo.14709141.

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Synthesis of substituted thiocarbamide derivatives is important in the fields of medicinal, agricultural, chemical, and pharmaceutical. Thiocarbamides are commonly utilized as starting materials for several organic synthetic processes and have been studied in search for easy and effective methods of chemical synthesis. In the existing research work, 3-chloroaniline was protected by a di-tert-butyl dicarbonate (BoC) protecting agent. Substituted thiocarbamide derivatives were synthesized using condensation of various substituted thioureas with amino group-protected 3-chloroaniline. The structur

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17

A., RAMESH, KRISHNAMACHARYULU J., K. RAVINDRANATH L., and BRAHMAJI RAO S. "Electrochemical Behaviour of Substituted-N-aryl-N1-2-( 4-p-anisyl-5-arylazothiazolyl)thiocarbamides." Journal of Indian Chemical Society Vol. 68, Oct 1991 (1991): 545–48. https://doi.org/10.5281/zenodo.5969635.

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Department of Chemistry, J.N.T.U. College of Engineering, Anantapnr-515 002 Department of Chemistry, S. K. University, Anantapur-515 003 <em>Manuscript received 30 March 1990, revised 26 August 1991, accepted 20 September 1991</em> <em>N</em>-Aryl-<em>N</em><sup>1</sup>-2 (4-<em>p</em>-anisyl-5- arylazothiazolyl)thiocarbamides (1-5) exhibit a well-defined reduction wave at DME and a cathodic peak at HMDE in Britton-Robinson butlers (pH 20 -10.0) containing 60% (v/v) dimethylformamide. The products of electrolysis have been characterised and a plausible mechanism has been suggested.

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18

Kavita, M. Heda, та P. Deshmukh Shirish. "Synthesis and biological evaluation of 4-aryl-5-hepta-O-benzoyl-β-D-lactosylimino¬3-hepta-O-benzoyl-β-D-lactosylimino-l,2,4-dithiazolidines (hydrochlorides)". Journal of Indian Chemical Society Vol. 93, Dec 2016 (2016): 1413–16. https://doi.org/10.5281/zenodo.5599109.

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Department of Chemistry, Shri R. L. T. College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : kavitaheda25@gmail.com P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>Manuscript received 04 November 2015, accepted 26 October 2016</em> A series of 4-aryl-5-hepta-<em>O</em>-benzoyl-β-D-lactosylimino-3-hepta-<em>O</em>-benzoyl-β-D-lactosylimino-1,2,4-dithiazolidines (hydrochloride) have been synthesized by the interaction of various 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-3-aryl thiocarbamides with <em>N</em>-hepta-<em>O</em>

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19

Pradip, P. Deohate, P. Deohatc Jyoti, and N. Berad B. "Synthesis of novel benzo-1,2,5-thiadiazines, their antimicrobial activity and isomerization into benzo-1,2,4-triazines." Journal of India Chemical Society Vol 81, Sep 2004 (2004): 775–77. https://doi.org/10.5281/zenodo.5833095.

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P. G. Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, India <em>E-mail</em>: pradip222091 @yahoo.co.in <em>Manuscript received 23 April 2003. revised 12 March 2004. accepted 6 April 2004</em> Benzo[<em>c</em>]-6-aryl/alkylimino-1,2,5-thiadiazines (4a-g) have been obtained by the basification of benzo[<em>c</em>]-6-aryl/alkylimino-1 ,2,5- thiadiazine dihydroiodides (3a-g). The latter were synthesized by the oxidative cyclisation of substituted 1-aryl/alkyl- 3-(2' -aminophenyl)thiocarbamides (2a-g) by ethanolic iodine. Compounds (4a-g) on acylation with acetic anhydr

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20

P., V. Tale, та P. Deshmukh S. "Synthesis of 3-hepta-O-acetyl-β-lactosylimino-4-aryl-5-phenylimino1 ,2,4-dithiazolidines (hydrochlorides)". Journal of Indian Chemical Society Vol. 84, Oct 2007 (2007): 1029–31. https://doi.org/10.5281/zenodo.5827174.

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P. G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em>: prashanttale@rediffmail.com <em>Manuscript received 14 February 2007, revised 10 April 2007, accepted 20 July 2007</em> Some 3-hepta-<em>O</em>-acetyl-β-lactosylimino-4-aryl-5-phenylimino-1,2,4-dithiazolidines (hydrochlorides) (3) have been synthesized for the first time involving interaction of 1-hepta-<em>O</em>-acetyl-β-D-lactosyl-3-aryl thiocarbamnides (1) and <em>N</em>-phenyl-<em>S</em>-chloro isothiocarbomyl chloride (2).

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21

Kumar M, Rajesh, Manikandan Alagumuthu, and Violet Dhayabaran V. "Synthesis and Molecular Drug Efficacy of Indoline-based Dihydroxy-thiocarbamides: Inflammation Regulatory Property Unveiled over COX-2 Inhibition, Molecular Docking, and Cytotoxicity Prospects." Journal of Heterocyclic Chemistry 55, no. 7 (2018): 1658–68. http://dx.doi.org/10.1002/jhet.3201.

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22

Cram, Donald J. "Molecular container compounds." Nature 356, no. 6364 (1992): 29–36. http://dx.doi.org/10.1038/356029a0.

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23

Pinheiro, C. B. "Modulated molecular compounds." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (2011): C192. http://dx.doi.org/10.1107/s0108767311095213.

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24

ORITA, Yoshimasa, and Akio ANDO. "(1)Small Molecular Compounds." Japanese Journal of Medicine 26, no. 2 (1987): 278–80. http://dx.doi.org/10.2169/internalmedicine1962.26.278.

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25

Yakovishin, L. A., N. I. Borisenko, E. V. Vetrova, M. I. Rudnev, and V. I. Grishkovets. "Low-Molecular-Weight Compounds." Russian Journal of Bioorganic Chemistry 37, no. 7 (2011): 858–61. http://dx.doi.org/10.1134/s1068162011070260.

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26

Roggan, Stefan, and Christian Limberg. "Molecular molybdenum/bismuth compounds." Inorganica Chimica Acta 359, no. 15 (2006): 4698–722. http://dx.doi.org/10.1016/j.ica.2006.04.030.

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27

Cañadillas-Delgado, Laura, Fernando S. Delgado-Trujillo, Óscar Fabelo, et al. "Heterobimetallic malonate-containing molecular compounds." Acta Crystallographica Section A Foundations of Crystallography 65, a1 (2009): s285. http://dx.doi.org/10.1107/s0108767309093970.

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28

Mao, W., and H. Mao. "Hydrogen storage in molecular compounds." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (2005): c63. http://dx.doi.org/10.1107/s010876730509731x.

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29

Edkins, Katharina. "Molecular interactions in pharmaceutical compounds." Acta Crystallographica Section A Foundations and Advances 72, a1 (2016): s43. http://dx.doi.org/10.1107/s2053273316099344.

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30

Mao, W. L., and H. k. Mao. "Hydrogen storage in molecular compounds." Proceedings of the National Academy of Sciences 101, no. 3 (2004): 708–10. http://dx.doi.org/10.1073/pnas.0307449100.

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31

Abraham, R. J., and G. H. Grant. "Molecular modeling of silicon compounds." Journal of Molecular Graphics 6, no. 4 (1988): 217. http://dx.doi.org/10.1016/s0263-7855(98)80025-8.

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32

SATO, O. "Photoinduced magnetization in molecular compounds." Journal of Photochemistry and Photobiology C: Photochemistry Reviews 5, no. 3 (2004): 203–23. http://dx.doi.org/10.1016/j.jphotochemrev.2004.10.001.

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33

J.L.S. "Molecular modelling of inorganic compounds." Journal of Molecular Structure 382, no. 3 (1996): 216–17. http://dx.doi.org/10.1016/0022-2860(96)83684-2.

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34

Hoyer, E. "Molecular Modeling of Inorganic Compounds." Zeitschrift für Physikalische Chemie 196, Part_1 (1996): 158. http://dx.doi.org/10.1524/zpch.1996.196.part_1.158.

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35

D.W.H.R. "Molecular Structure of Organosilicon Compounds." Journal of Molecular Structure 245, no. 1-2 (1991): 159–60. http://dx.doi.org/10.1016/0022-2860(91)87017-c.

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36

Chaloner, Penny A. "Molecular Design of Tautomeric Compounds." Coordination Chemistry Reviews 89 (September 1988): 313–16. http://dx.doi.org/10.1016/0010-8545(88)80038-9.

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37

Eaborn, Colin. "Molecular Structure of Organosilicon Compounds." Journal of Organometallic Chemistry 391, no. 2 (1990): C34—C35. http://dx.doi.org/10.1016/0022-328x(90)80186-4.

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38

Engström, L. "Triglyceride Systems Forming Molecular Compounds." Fett Wissenschaft Technologie/Fat Science Technology 94, no. 5 (1992): 173–81. http://dx.doi.org/10.1002/lipi.19920940503.

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39

Pandi, Sangavi, Langeswaran Kulanthaivel, Gowtham Kumar Subbaraj, Sangeetha Rajaram, and Senthilkumar Subramanian. "Screening of Potential Breast Cancer Inhibitors through Molecular Docking and Molecular Dynamics Simulation." BioMed Research International 2022 (June 28, 2022): 1–9. http://dx.doi.org/10.1155/2022/3338549.

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Cyclooxygenase-2 (COX-2) is a key enzyme involved in overexpression in several human cancerous diseases including breast cancer. By performing efficient virtual screening in a series of active molecules or compounds from the Maybridge, NCI (National Cancer Institute), and Enamine databases, potential identification of COX-2 inhibitors could lead to new prognostic strategies in the treatment of breast cancer. Based on a 50% structural similitude, compounds were chosen as the inductive model of COX-2 inhibitions from these databases. Selected compounds were filtered and tested with Lipinski’s ru

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40

Gupta, Sakuntala. "Molecular packing of mesogenic bicyclohexylnitrile compounds." Acta Crystallographica Section A Foundations and Advances 77, a2 (2021): C1031. http://dx.doi.org/10.1107/s0108767321086700.

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41

OONISHI, Isao, and Shoji FUJISAWA. "Molecular deformation of polycyclic aromatic compounds." Nihon Kessho Gakkaishi 32, no. 4 (1990): 207–12. http://dx.doi.org/10.5940/jcrsj.32.207.

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42

McKelvy, M. J., and W. S. Glaunsinger. "Molecular Intercalation Reactions in Lamellar Compounds." Annual Review of Physical Chemistry 41, no. 1 (1990): 497–523. http://dx.doi.org/10.1146/annurev.pc.41.100190.002433.

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43

Li, Shusen, and Chengye Yuan. "Molecular Mechanics Study of Organophosphorus Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 147, no. 1 (1999): 209. http://dx.doi.org/10.1080/10426509908053585.

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44

SATOH, Takumi. "Neurotrophin-like low molecular weight compounds." Folia Pharmacologica Japonica 120, no. 5 (2002): 327–34. http://dx.doi.org/10.1254/fpj.120.327.

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45

Ribou, A. C., T. Wada, and H. Sasabe. "Molecular design of asymmetric bichromophoric compounds." Synthetic Metals 81, no. 2-3 (1996): 277–80. http://dx.doi.org/10.1016/s0379-6779(96)03737-x.

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46

Bayse, Craig A., and Sonia Antony. "Molecular modeling of bioactive selenium compounds." Main Group Chemistry 6, no. 3-4 (2007): 185–200. http://dx.doi.org/10.1080/10241220801994700.

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47

CAO, Xiaoyan. "Molecular structure of diatomic lanthanide compounds." Science in China Series B 45, no. 1 (2002): 91. http://dx.doi.org/10.1360/02yb9013.

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48

Asakawa, Masumi, Dario Pasini, Françisco M. Raymo, and J. Fraser Stoddart. "Chromatography of Mechanically Interlocked Molecular Compounds." Analytical Chemistry 68, no. 21 (1996): 3879–81. http://dx.doi.org/10.1021/ac9604604.

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Schweizer, J. "Spin densities in magnetic molecular compounds." Physica B: Condensed Matter 234-236 (June 1997): 772–79. http://dx.doi.org/10.1016/s0921-4526(96)01162-3.

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Coleman, William F. "Molecular Models of Compounds in Lightsticks." Journal of Chemical Education 86, no. 1 (2009): 128. http://dx.doi.org/10.1021/ed086p128.

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