Log in

Relevant bibliographies by topics / Organotin carboxylates / Journal articles

To see the other types of publications on this topic, follow the link: Organotin carboxylates.

Journal articles on the topic 'Organotin carboxylates'

Author: Grafiati

Published: 18 May 2024

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Organotin carboxylates.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Hussain, Mukhtiar, Muhammad Zaman, Muhammad Hanif, Saqib Ali, and Muhammad Danish. "Synthesis and structural characterization of organotin(IV) complexes formed with [o,o] donor atoms of carboxylic acids." Journal of the Serbian Chemical Society 73, no. 2 (2008): 179–87. http://dx.doi.org/10.2298/jsc0802179h.

Full text

Abstract:

Organotin(IV) carboxylates of the general formula RnSnL4-n (where R = Me, n-Bu or Ph, and L = ?-phenyl-2,3-(methylenedioxy)cinnamate anion or 2-(2,3-dimethlylanilino)nicotinate anion) have been prepared. The mono-, di- and tri-organotin(IV) carboxylates were synthesized by the reaction of organotin(IV) oxides or hydroxides with a stoichiometric amount of the ligand acids at an elevated temperature in dry toluene. The composition of the synthesized organotin(IV) complexes, the bonding behavior of the donor groups and structural assignments were studied by elemental analysis, FT-IR, 1H-, 13C-NMR and mass spectrometry. The spectral data suggest that the ligand acts in a bidentate manner, coordinating through the oxygen atoms. These spectroscopic techniques revealed a distorted tetrahedral geometry in the solution state for the tri-organotins, while a mean coordination number between five to six for the diorganotin(IV) dicarboxylates. In the solid phase, the tri-organotins were essentially trigonal bipyramidal polymeric while the di-organotins were octa?hedral. However, mono-organotin tricarboxylates were predicted to exist in the octahedral state both in solution as well as in the solid phase.

APA, Harvard, Vancouver, ISO, and other styles

2

Mazhar, M., M. Aziz Choudhary, Saqib Ali, Qing-Lan Xie, and Xueqing Song. "ChemInform Abstract: Organotin Carboxylates." ChemInform 33, no. 17 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200217255.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Bonire, Josiah J., G. Adefikayo Ayoko, Philip F. Olurinola, Joseph O. Ehinmidu, Neelam S. N. Jalil, and Andrew A. Omachi. "Synthesis and Antifungal Activity of Some Organotin(IV) Carboxylates." Metal-Based Drugs 5, no. 4 (January 1, 1998): 233–36. http://dx.doi.org/10.1155/mbd.1998.233.

Full text

Abstract:

Six diorganotin(IV) carboxylates prepared by reacting diorganotin(IV) dichlorides with the respective silver carboxylate have been tested for antifungal activity against Aspergillus. niger, Aspergilluus flavus and Pencillium. citrinum in Sabourand dextrose broth. The compounds generally exhibit greater fungitoxicity than the diorganotin(IV) dichlorides and the carboxylic acids from which they were synthesized. In keeping with the generally accepted notion that the organotin moiety plays an important role in deciding the antifungal activity of an organotin compound, the diphenyltin(IV) compounds were more active than their di-n-butyltin(IV) analogues. However, the order of increasing fungitoxicity of the compounds parallels that of the uncomplexed carboxylic acids. The implications of the results are discussed.

APA, Harvard, Vancouver, ISO, and other styles

4

Sandhu, Gurmit K., Neelam Sharma, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 371, no. 1 (July 1989): C1—C3. http://dx.doi.org/10.1016/0022-328x(89)85215-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Parulekar, C. S., V. K. Jain, T. K. Das, A. R. Gupta, B. F. Hoskins, and E. R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 372, no. 2 (August 1989): 193–99. http://dx.doi.org/10.1016/0022-328x(89)87093-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Sandhu, G. K., S. P. Verma, and E. R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 393, no. 2 (August 1990): 195–200. http://dx.doi.org/10.1016/0022-328x(90)80198-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Vatsa, Charu, Vimal K. Jain, T. Kesavadas, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 410, no. 2 (June 1991): 135–42. http://dx.doi.org/10.1016/0022-328x(91)80002-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Ng, Seik Weng, V. G. Kumar Das, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 403, no. 1-2 (February 1991): 111–17. http://dx.doi.org/10.1016/0022-328x(91)83092-i.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Sandhu, Gurmit K., Neelam Sharma, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 403, no. 1-2 (February 1991): 119–31. http://dx.doi.org/10.1016/0022-328x(91)83093-j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Tiekink, Edward R. T. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 408, no. 3 (May 1991): 323–27. http://dx.doi.org/10.1016/0022-328x(91)83203-g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Ng, Seik Weng, V. G. Kumar Das, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 411, no. 1-2 (July 1991): 121–29. http://dx.doi.org/10.1016/0022-328x(91)86011-e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Sandhu, Gurmit K., Rajbir Hundal, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 412, no. 1-2 (July 1991): 31–38. http://dx.doi.org/10.1016/0022-328x(91)86038-r.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Vatsa, Charu, Vimal K. Jain, T. Kesavadas, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 408, no. 2 (May 1991): 157–66. http://dx.doi.org/10.1016/0022-328x(91)86379-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Vasta, C., V. K. Jain, T. K. Das, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 421, no. 1 (December 1991): 21–28. http://dx.doi.org/10.1016/0022-328x(91)86428-s.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Sandhu, Gurmit K., Rajbir Hundal, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 430, no. 1 (June 1992): 15–23. http://dx.doi.org/10.1016/0022-328x(92)80091-b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Mokal, V. B., Vimal K. Jain, and Edward R. T. Tiekink. "Structural chemistry of organotin carboxylates." Journal of Organometallic Chemistry 431, no. 3 (July 1992): 283–88. http://dx.doi.org/10.1016/0022-328x(92)83332-c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Amir, Muhammad Kashif, Shahanzeb Khan, Zia-ur-Rehman, Afzal Shah, and Ian S. Butler. "Anticancer activity of organotin(IV) carboxylates." Inorganica Chimica Acta 423 (November 2014): 14–25. http://dx.doi.org/10.1016/j.ica.2014.07.053.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Devendra, Ransi, Neil R. Edmonds, and Tilo Söhnel. "Organotin carboxylate catalyst in urethane formation in a polar solvent: an experimental and computational study." RSC Advances 5, no. 60 (2015): 48935–45. http://dx.doi.org/10.1039/c5ra03367e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Xiao, Xiao, Wenliang Li, Chengwu Liang, and Wenxiu Zhao. "Organotin carboxylates: from structures to antitumour activities." European Journal of BioMedical Research 1, no. 4 (December 28, 2015): 23. http://dx.doi.org/10.18088/ejbmr.1.4.2015.pp23-27.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Hussain, Shabbir, Saqib Ali, Saira Shahzadi, Saroj K. Sharma, Kushal Qanungo, and Muhammad Shahid. "Synthesis, Characterization, Semiempirical and Biological Activities of Organotin(IV) Carboxylates with 4-Piperidinecarboxylic Acid." Bioinorganic Chemistry and Applications 2014 (2014): 1–11. http://dx.doi.org/10.1155/2014/959203.

Full text

Abstract:

Organotin (IV) carboxylates with the general formulae R2Sn(Cl)L [R = Me (1),n-Bu (2), Ph (3)] and R3SnL [R = Me (4), Ph (5)] have been synthesized by the reaction of 4-piperidinecarboxylic acid (HL) with KOH and R2SnCl2(R = Me,n-Bu, Ph)/R3SnCl (R = Me, Ph) in methanol under stirring conditions. The metal ligand binding site, structure, and stability of complexes have been verified by FT-IR, (1H,13C) NMR, EI-MS technique, and semiempirical study. The FT-IR data indicate the bidentate chelating mode of the carboxylate ligand which is also confirmed by semiempirical study. In solution state, five and four coordinated geometry around tin was confirmed by NMR spectroscopy. The EI-MS data agreed well with the molecular structure of the complexes. Thermodynamic parameters and molecular descriptors were calculated by using semiempirical PM3 method. HOMO-LUMO calculations show that chlorodiorganotin complexes are more susceptible to nucleophilic attack as compared to triorganotin complexes. Computed negative heat of formation indicates that complexes1–4are thermodynamically stable. The organotin(IV) carboxylates displayed powerful antimicrobial activities against various strains of bacteria and fungi and their minimal inhibitory concentration were also evaluated. The complexes exhibited comparatively higher hemolytic activity as compared to free ligand.

APA, Harvard, Vancouver, ISO, and other styles

21

Petrosyan, V. S., N. S. Yashina, S. V. Ponomarev, A. S. Zolotareva, S. N. Nikolaeva, and Τ. V. Drovetskaia. "THE COMPARATIVE STUDIES OF ORGANOTIN AND ORGANOGERMANIUM CARBOXYLATES." Main Group Metal Chemistry 19, no. 6 (January 1996): 397–408. http://dx.doi.org/10.1515/mgmc.1996.19.6.397.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Predarska, Ivana, Mohamad Saoud, Ibrahim Morgan, Peter Lönnecke, Goran N. Kaluđerović, and Evamarie Hey-Hawkins. "Triphenyltin(IV) Carboxylates with Exceptionally High Cytotoxicity against Different Breast Cancer Cell Lines." Biomolecules 13, no. 4 (March 26, 2023): 595. http://dx.doi.org/10.3390/biom13040595.

Full text

Abstract:

Organotin(IV) carboxylates are a class of compounds explored as alternatives to platinum-containing chemotherapeutics due to propitious in vitro and in vivo results, and distinct mechanisms of action. In this study, triphenyltin(IV) derivatives of non-steroidal anti-inflammatory drugs (indomethacin (HIND) and flurbiprofen (HFBP)) are synthesized and characterized, namely [Ph3Sn(IND)] and [Ph3Sn(FBP)]. The crystal structure of [Ph3Sn(IND)] reveals penta-coordination of the central tin atom with almost perfect trigonal bipyramidal geometry with phenyl groups in the equatorial positions and two axially located oxygen atoms belonging to two distinct carboxylato (IND) ligands leading to formation of a coordination polymer with bridging carboxylato ligands. Employing MTT and CV probes, the antiproliferative effects of both organotin(IV) complexes, indomethacin, and flurbiprofen were evaluated on different breast carcinoma cells (BT-474, MDA-MB-468, MCF-7 and HCC1937). [Ph3Sn(IND)] and [Ph3Sn(FBP)], unlike the inactive ligand precursors, were found extremely active towards all examined cell lines, demonstrating IC50 concentrations in the range of 0.076–0.200 µM. Flow cytometry was employed to examine the mode of action showing that neither apoptotic nor autophagic mechanisms were triggered within the first 48 h of treatment. However, both tin(IV) complexes inhibited cell proliferation potentially related to the dramatic reduction in NO production, resulting from downregulation of nitric oxide synthase (iNOS) enzyme expression.

APA, Harvard, Vancouver, ISO, and other styles

23

Abbas, Syed Mustansar, Saqib Ali, Syed Tajammul Hussain, and Saira Shahzadi. "Review: structural diversity in organotin(IV) dithiocarboxylates and carboxylates." Journal of Coordination Chemistry 66, no. 13 (June 11, 2013): 2217–34. http://dx.doi.org/10.1080/00958972.2013.802310.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

G. Hadi, Angham, Khudheir Jawad, Dina S. Ahmed, and Emad Yousif. "Synthesis and Biological Activities of Organotin (IV) Carboxylates: A Review." Systematic Reviews in Pharmacy 10, no. 1 (December 14, 2018): 26–31. http://dx.doi.org/10.5530/srp.2019.1.5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Molloy, Kieran C. "Solid state 119Sn NMR study of organotin carboxylates and thiophosphates." Inorganica Chimica Acta 141, no. 2 (January 1988): 151–52. http://dx.doi.org/10.1016/s0020-1693(00)83897-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Del Re, Ryan, James Passarelli, Miriam Sortland, Brian Cardineau, Yasin Ekinci, Elizabeth Buitrago, Mark Neisser, Daniel A. Freedman, and Robert L. Brainard. "Low-line edge roughness extreme ultraviolet photoresists of organotin carboxylates." Journal of Micro/Nanolithography, MEMS, and MOEMS 14, no. 4 (November 9, 2015): 043506. http://dx.doi.org/10.1117/1.jmm.14.4.043506.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Liu, Dong, Wen-Can Chen, Guo-Li Shen, and Ru-Qin Yu. "Polymeric membrane salicylate-sensitive electrodes based on organotin(IV) carboxylates." Analyst 121, no. 10 (1996): 1495. http://dx.doi.org/10.1039/an9962101495.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

PETROSYAN, V. S., N. S. YASHINA, S. V. PONOMAREV, A. S. ZOLOTAREVA, S. N. NIKOLAEVA, and T. V. DROVETSKAIA. "ChemInform Abstract: The Comparative Studies of Organotin and Organogermanium Carboxylates." ChemInform 27, no. 50 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199650253.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Levent, Emre, Oliver Sala, Lukas F. B. Wilm, Pawel Löwe, and Fabian Dielmann. "Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts – alternatives to organotin compounds." Green Chemistry 23, no. 7 (2021): 2747–55. http://dx.doi.org/10.1039/d1gc00446h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Vinayak, Richa, and Hari Pada Nayek. "Selective sensing of a Cu(ii) ion by organotin anchored keto-enamine ligands." New Journal of Chemistry 43, no. 40 (2019): 16050–57. http://dx.doi.org/10.1039/c9nj03204e.

Full text

Abstract:

New organotin carboxylates [{(n-Bu)₂Sn(HL)}₂O]₂ (1), [(t-Bu)₂Sn(HL)₂] (2) and [Ph₃Sn(HL)] (3) have been synthesized and used for sensing of Cu(ii) ion. Complex 3 shows highest binding constant and better limit of detection than other complexes.

APA, Harvard, Vancouver, ISO, and other styles

31

Vinayak, Richa, and Hari Pada Nayek. "Organotin metalloligands for selective sensing of metal ions." New Journal of Chemistry 43, no. 19 (2019): 7259–68. http://dx.doi.org/10.1039/c9nj00944b.

Full text

Abstract:

Four new organotin carboxylates, [(t-C₄H₉)₂Sn(L₁)₂] (1), [(t-C₄H₉)₂Sn(L₂)₂] (2), [{(n-C₄H₉)₂Sn(L₁)}₂O]₂ (3) and [{(n-C₄H₉)₂Sn(L₂)}₂O]₂ (4), are reported. All complexes selectively recognize Cu(ii) and Fe(iii) ions in solution. Complex 1 was found to be the best one for sensing those ions among all complexes.

APA, Harvard, Vancouver, ISO, and other styles

32

Salma, U., Imtiaz-ud-Din, M. Mazhar, and Khalid Mohammed Khan. "Germatranyl Substituted Organotin (IV) Carboxylates: Synthesis Spectroscopic Characterization and Biological Activities." Medicinal Chemistry 5, no. 6 (November 1, 2009): 543–48. http://dx.doi.org/10.2174/157340609790170489.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Iqbal, Muhammad, Saqib Ali, Niaz Muhammad, Masood Parvez, Peter Langer, and Alexander Villinger. "Synthesis, characterization, crystal structures and electrochemical studies of organotin(IV) carboxylates." Journal of Organometallic Chemistry 723 (January 2013): 214–23. http://dx.doi.org/10.1016/j.jorganchem.2012.10.006.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Danish, M., N. Ahmad, N. Zahara, S. Ali, and N. Muhammad. "Thermokinetic studies of organotin(IV) carboxylates derived from para-methoxyphenylethanoic acid." Journal of the Iranian Chemical Society 7, no. 4 (December 2010): 846–52. http://dx.doi.org/10.1007/bf03246078.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Xiao, Xiao, Lisong Yan, Zemin Mei, Dongsheng Zhu, and Lin Xu. "Two novel macrocyclic organotin(iv) carboxylates based on amide carboxylic acids." RSC Adv. 4, no. 6 (2014): 3096–101. http://dx.doi.org/10.1039/c3ra46198j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Sakho, Adama Moussa, Dafeng Du, Wenjie Li, Shuangshuang Liu, Dongsheng Zhu, and Lin Xu. "Synthesis, crystal structures, and antitumor activity of three new organotin carboxylates." Heteroatom Chemistry 21, no. 5 (June 22, 2010): 304–13. http://dx.doi.org/10.1002/hc.20614.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Abbas, Syed Mustansar, Saqib Ali, Syed Tajammul Hussain, and Saira Shahzadi. "ChemInform Abstract: Review: Structural Diversity in Organotin(IV) Dithiocarboxylates and Carboxylates." ChemInform 44, no. 49 (November 14, 2013): no. http://dx.doi.org/10.1002/chin.201349225.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Tiekink, Edward R. T. "Structural chemistry of organotin carboxylates: a review of the crystallographic literature." Applied Organometallic Chemistry 5, no. 1 (January 1991): 1–23. http://dx.doi.org/10.1002/aoc.590050102.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Wang, Zhi-Hong, Yan-Zhao Guo, Jun Zhang, Lin Ma, Hai-Bin Song, and Zhi-Jin Fan. "Synthesis and Biological Activity of Organotin 4-Methyl-1,2,3-thiadiazole-5-carboxylates and Benzo[1,2,3]thiadiazole-7-carboxylates†." Journal of Agricultural and Food Chemistry 58, no. 5 (March 10, 2010): 2715–19. http://dx.doi.org/10.1021/jf902168d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Ahmet, Mustafa T., Andrew Houlton, Christopher S. Frampton, John R. Miller, Roger M. G. Roberts, Jack Silver, and Bahram Yavari. "Tin-119 Mössbauer and nuclear magnetic resonance studies of organotin compounds. Part 2. Sterically crowded organotin halides and carboxylates." J. Chem. Soc., Dalton Trans., no. 20 (1993): 3085–92. http://dx.doi.org/10.1039/dt9930003085.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

AHMET, M. T., A. HOULTON, C. S. FRAMPTON, J. R. MILLER, R. M. G. ROBERTS, J. SILVER, and B. YAVARI. "ChemInform Abstract: Tin-119 Moessbauer and NMR Studies of Organotin Compounds. Part 2. Sterically Crowded Organotin Halides and Carboxylates." ChemInform 25, no. 5 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199405030.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Zhang, Yuan-Yuan, Ru-Fen Zhang, Shao-Liang Zhang, Shuang Cheng, Qian-Li Li, and Chun-Lin Ma. "Syntheses, structures and anti-tumor activity of four new organotin(iv) carboxylates based on 2-thienylselenoacetic acid." Dalton Transactions 45, no. 20 (2016): 8412–21. http://dx.doi.org/10.1039/c6dt00532b.

Full text

Abstract:

With the 2-thienylselenoacetic acid ligand, four new organotin complexes have been synthesized and characterized by X-ray crystallography, elemental analysis, FT-IR and NMR (¹H,¹³C, and¹¹⁹Sn) spectroscopy.

APA, Harvard, Vancouver, ISO, and other styles

43

Geng, Wen-Qian, Hong-Ping Zhou, Long-Huai Cheng, Fu-Ying Hao, Guo-Yi Xu, Fei-Xia Zhou, Zhi-Peng Yu, et al. "Synthesis and structural characterization of organotin(IV) carboxylates based on different heterocyclic substituents." Polyhedron 31, no. 1 (January 2012): 738–47. http://dx.doi.org/10.1016/j.poly.2011.10.032.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Xiao, Xiao, Dafeng Du, Min Tian, Xiao Han, Jingwen Liang, Dongsheng Zhu, and Lin Xu. "Organotin(IV) carboxylates based on benzenedicarboxylic acid derivatives: Syntheses, crystal structures and characterizations." Journal of Organometallic Chemistry 715 (September 2012): 54–63. http://dx.doi.org/10.1016/j.jorganchem.2012.05.038.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Xiao, Xiao, Xiao Han, Zemin Mei, Dongsheng Zhu, Kuizhan Shao, Jingwen Liang, Min Tian, and Lin Xu. "Organotin(IV) carboxylates based on amide carboxylic acids: Syntheses, crystal structures and characterizations." Journal of Organometallic Chemistry 729 (April 2013): 28–39. http://dx.doi.org/10.1016/j.jorganchem.2013.01.017.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

TIEKNIK, E. R. T. "ChemInform Abstract: Structural Chemistry of Organotin Carboxylates: A Review of the Crystallographic Literature." ChemInform 23, no. 21 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199221322.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Blunden, S. J., R. Hill, and S. E. Sutton. "A thermal analytical study of some mono- and di-organotin oxides and carboxylates." Applied Organometallic Chemistry 5, no. 3 (May 1991): 159–65. http://dx.doi.org/10.1002/aoc.590050304.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Dyląg, Mariusz, Hanna Pruchnik, Florian Pruchnik, Grażyna Majkowska-Skrobek, and Stanisław Ułaszewski. "Antifungal activity of organotin compounds with functionalized carboxylates evaluated by the microdilution bioassayin vitro." Medical Mycology 48, no. 2 (March 2010): 373–83. http://dx.doi.org/10.3109/13693780903188680.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Sirajuddin, Muhammad, and Saqib Ali. "Organotin(IV) Carboxylates as Promising Potential Drug Candidates in the Field of Cancer Chemotherapy." Current Pharmaceutical Design 22, no. 44 (January 13, 2017): 6665–81. http://dx.doi.org/10.2174/1381612822666160906143249.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Kang, Wanli, Xiaoyan Wu, and Jianbin Huang. "Synthesis, crystal structure and biological activities of four novel tetranuclear di-organotin(IV) carboxylates." Journal of Organometallic Chemistry 694, no. 15 (July 2009): 2402–8. http://dx.doi.org/10.1016/j.jorganchem.2009.03.025.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!