Synthesis of Halogen-Substituted [12]Mercuracarborands-4. Crystal Structure of {[(9,12-I2-C2B10H8-1,2-Hg)4]Cl}Na(H2O)n
- Авторлар: Suponitsky K.Y.1, Anufriev S.A.2, Shmalko A.V.2, Sivaev I.B.2
-
Мекемелер:
- Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
- Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Шығарылым: Том 50, № 5 (2024)
- Беттер: 344-352
- Бөлім: Articles
- URL: https://medjrf.com/0132-344X/article/view/667601
- DOI: https://doi.org/10.31857/S0132344X24050066
- EDN: https://elibrary.ru/NJYNCZ
- ID: 667601
Дәйексөз келтіру
Аннотация
The reactions of the dilithium derivatives of 9,12-dihalogen-ortho-carboranes 1,2-Li2-C2B10H8-9,12-X2 (X = Cl, Br, I) with mercury chloride HgCl2 afford a number of complexes of the chloride ion with the halogen derivatives of [12] mercuracarborand-4: {[(9,12-X2-C2B10H8-1,2ʹ-Hg)4]Cl}Na · nH2O. The molecular crystal structure of the complex of the
[12]mercuracarborand-4 octaiodine derivative with the chloride ion is determined by X-ray diffraction. The substituents at the periphery of the mercury-containing macrocycle are found to exert a substantial effect on the macrocycle geometry leading to the transition from the planar to butterfly conformation, whose geometry is predetermined by a set of intermolecular interactions in the crystal.
Негізгі сөздер
Толық мәтін

Авторлар туралы
K. Suponitsky
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: kirshik@yahoo.com
Ресей, Moscow
S. Anufriev
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: kirshik@yahoo.com
Ресей, Moscow
A. Shmalko
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: kirshik@yahoo.com
Ресей, Moscow
I. Sivaev
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: sivaev@ineos.ac.ru
Ресей, Moscow
Әдебиет тізімі
- Frankland, E., Philos. Trans., 1852, vol. 142, p. 417. https://www.jstor.org/stable/108548
- Frankland, E., Ann., 1853, vol. 85, no. 3, p. 329. https://doi.org/10.1002/jlac.18530850308
- Frankland, E. and Duppa, B.F., J. Chem. Soc., 1863, vol. 16, p. 415. https://doi.org/10.1039/JS8631600415
- Frankland, E. and Duppa, B.F., Ann., 1864, vol. 130, no. 1, p. 104. https://doi.org/10.1002/jlac.18641300110
- Geier, D.A., King, P.G., Hooker, B.S., et al., Clin. Chim. Acta, 2015, vol. 444, p. 212. https://doi.org/10.1016/j.cca.2015.02.030
- Makarova, L.G. and Nesmeyanov, A.N., Methods of Elemento-organic Chemistry. Vol. 4. The Organic Compounds of Mercury, Amsterdam, 1967.
- Kuzʹmina, L.G. and Struchkov, Yu.T., Croat. Chem. Acta, 1984, vol. 57, no. 4, p. 701. https://hrcak.srce.hr/194141
- Sivaev, I.B. and Stogniy, M.Yu., Russ. Chem. Bull., 2019, vol. 68, no. 2, p. 217. https://doi.org/10.1007/s11172-019-2379-5
- Pearce, K.G., Dinoi, C., Schwamm, R.J., et al., Adv. Sci., 2023, vol. 10, no. 31, p. 2304765. https://doi.org/10.1002/advs.202304765
- Larock, R.C., Angew. Chem. Int. Ed., 1978, vol. 17, no. 1, p. 27. https://doi.org/10.1002/anie.197800271
- Taylor, T.J., Burress, C.N., and Gabbai, F.P., Organometallics, 2007, vol. 26, no. 22, p. 5252. https://doi.org/10.1021/om070125d
- Yakovenko, A.A., Gallegos, J.H., Antipin, M.Yu., and Timofeeva, T.V., Cryst. Growth Des., 2009, vol. 9, no. 1, p. 66. https://doi.org/10.1021/cg8006603
- Yakovenko, A.A., Gallegos, J.H., Antipin, M.Yu., et al., Cryst. Growth Des., 2011, vol. 11, no. 9, p. 3964. https://doi.org/10.1021/cg200547k
- Himmelspach, A., Zahres, M., and Finze, M., Inorg. Chem., 2011, vol. 50, no. 8, p. 3186. https://doi.org/10.1021/ic200330d
- Shur, V.B. and Tikhonova, I.A., Russ. Chem. Bull., 2003, vol. 52, no. 12, p. 2539. https://doi.org/10.1023/B:RUCB.0000019872.65342.9a
- Dolgushin, F.M. and Eremenko, I.L., Russ. Chem. Rev., 2021, vol. 90, no. 12, p. 1493. https://doi.org/10.1070/rcr4998
- Avdeeva, V.V., Malinina, E.A., and Kuznetsov, N.T., Coord. Chem. Rev., 2022, vol. 469, p. 214636. https://doi.org/10.1016/j.ccr.2022.214636
- Loveday, O., Jover, J., and Echeverria, J., Inorg. Chem., 2022, vol. 61, no. 32, p. 12526. https://doi.org/10.1021/acs.inorgchem.2c00921
- Rozhkov, A.V., Katlenok, E.A., Zhmykhova, M.V., et al., Inorg. Chem. Front., 2023, vol. 10, no. 2, p. 493. https://doi.org/10.1039/D2QI02047E
- Wedge, T.J. and Hawthorne, M.F., Coord. Chem. Rev., 2003, vol. 240, nos. 1–2, p. 111. https://doi.org/10.1016/S0010-8545(02)00259-X
- Sivaev, I.B., Anufriev, S.A., and Shmalko, A.V., Inorg. Chim. Acta, 2023, vol. 547, p. 121339. https://doi.org/10.1016/j.ica.2022.121339
- Anufriev, S.A., Timofeev, S.V., Zhidkova, O.B., et al., Crystals, 2022, vol. 12, no. 9, 1251. https://doi.org/10.3390/cryst12091251
- Zhidkova, O.B., Druzina, A.A., Anufriev, S.A., et al., Molbank, 2022, vol. 2022, no. 1, p. M1347. https://doi.org/10.3390/M1347
- Zheng, Z., Jiang, W., Zinn, A.A., et al., Inorg. Chem., 1995, vol. 34, no. 8, p. 2095. https://doi.org/10.1021/ic00112a023
- Armarego, W.L.F. and Chai, C.L.L., Purification of Laboratory Chemicals, Burlington: Butterworth-Heinemann, 2009.
- APEX2 and SAINT, Madison: Bruker AXS Inc., 2014.
- Sheldrick, G.M., Acta Cryst., Sect. C: Struct. Chem., 2015, vol. 71, no. 1, p. 3. https://doi.org/10.1107/S2053229614024218
- Bayer, M.J., Jalisatgi, S.S., Smart, B., et al., Angew. Chem. Int. Ed., 2004, vol. 43, no. 14, p. 1854. https://doi.org/10.1002/anie.200352899
- Zinn, A.A., Knobler, C.B., Harwell, D.E., and Hawthorne, M.F., Inorg. Chem., 1999, vol. 38, no. 9, p. 2227. https://doi.org/10.1021/ic9811244
- Yang, X., Knobler, C.B., Zheng, Z., and Hawthorne, M.F., J. Am. Chem. Soc., 1994, vol. 116, no. 16, p. 7142. https://doi.org/10.1021/ja00095a018
- Lee, H., Knobler, C.B., and Hawthorne, M.F., Angew. Chem. Int. Ed., 2001, vol. 40, no. 11, p. 2124. https://doi.org/10.1002/1521-3773(20010601)40:11 <2124::AID-ANIE2124>3.0.CO;2-W
- Zheng, Z., Knobler, C.B., Mortimer, M.D., et al., Inorg. Chem., 1996, vol. 35, no. 5, p. 1235. https://doi.org/10.1021/ic951069o
- Zheng, Z., Knobler, C.B., and Hawthorne, M.F., J. Am. Chem. Soc., 1995, vol. 117, no. 18, p. 5105. https://doi.org/10.1021/ja00123a012
- Puga, A.V., Teixidor, F., Sillanpaa, R., et al., Chem. Eur. J., 2009, vol. 15, no. 38, p. 9764. https://doi.org/10.1002/chem.200900926
- Suponitsky, K.Yu., Anisimov, A.A., Anufriev, S.A., et al., Crystals, 2021, vol. 11, no. 4, p. 396. https://doi.org/10.3390/cryst11040396
- Suponitsky, K.Yu., Anufriev, S.A., and Sivaev, I.B., Molecules, 2023, vol. 28, no. 2, p. 875. https://doi.org/10.3390/molecules28020875
- Lu, Z., Vanga, M., Li, S., et al., Dalton Trans., 2023, vol. 52, no. 13, p. 3964. https://doi.org/10.1039/D2DT03725D
Қосымша файлдар
