Counterion and steric effects in self-assembled HgX 2-thioether coordination polymers

Crystal Growth and Design

Volumn 12, Issue 3, 2012, Pages 1579-1585

  Carnes, Matthew E ^a   Lindquist, Nathan R ^a   Zakharov, Lev N ^a   Johnson, Darren W ^a  

^a UNIVERSITY OF OREGON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COORDINATION POLYMERS; COUNTERIONS; DIHALIDES; DITHIOETHERS; EXTENDED NETWORKS; IDENTICAL CONDITIONS; ONE-DIMENSIONAL POLYMERS; PENDANT GROUPS; SELF-ASSEMBLED; STERIC EFFECT; STERICS; THIOETHERS;

MERCURY (METAL); MERCURY COMPOUNDS; STOICHIOMETRY; X RAY CRYSTALLOGRAPHY;

POLYMERS;

EID: 84863296655     PISSN: 15287483     EISSN: 15287505     Source Type: Journal    
DOI: 10.1021/cg201625c     Document Type: Article

References (30)

1. Melnick, J. G.; Yurkerwich, K.; Parkin, G. J. Am. Chem. Soc. 2010, 132, 647-655
2. Rooney, J. P. K. Toxicology 2007, 234, 145-156
3. George, G. N.; Prince, R. C.; Gailer, J.; Buttigieg, G. A.; Denton, M. B.; Harris, H. H.; Pickering, I. J. Chem. Res. Toxicol. 2004, 17, 999-1006
4. Guzzi, G.; La Porta, C. A. M. Toxicology 2008, 244, 1-12
5. Carter, T. G.; Yantasee, W.; Sangvanich, T.; Fryxell, G. E.; Johnson, D. W.; Addleman, R. S. Chem. Commun. 2008, 5583-5585
6. Hutchison, A. R.; Atwood, D. A. J. Chem. Crystallogr. 2003, 33, 631-645
7. Nolan, E. M.; Lippard, S. J. J. Mater. Chem. 2005, 15, 2778-2783
8. Fakhari, A. R.; Ganjali, M. R.; Shamsipur, M. Anal. Chem. 1997, 69, 3693-3696
9. Díez-Gil, C.; Martínez, R.; Ratera, I.; Hirsh, T.; Espinosa, A.; Tárraga, A.; Molina, P.; Wolfbeis, O. S.; Veciana, J. Chem. Commun. 2011, 47, 1842-1844
10. Morsali, A.; Masoomi, M. Y. Coord. Chem. Rev. 2009, 253, 1882-1905
11. Peindy, H. N.; Guyon, F.; Knorr, M.; Strohmann, C. Z. Anorg. Allg. Chem. 2005, 631, 2397-2400
12. Peindy, H. N.; Guyon, F.; Knorr, M.; Smith, A. B.; Farouq, J. A.; Islas, S. A.; Rabinovich, D.; Golen, J. A.; Strohmann, C. Inorg. Chem. Commun. 2005, 8, 479-482
13. Pitt, M. A.; Johnson, D. W. Chem. Soc. Rev. 2007, 36, 1441-1453
14. Cangelosi, V. M.; Pitt, M. A.; Vickaryous, W. J.; Allen, C. A.; Zakharov, L. N.; Johnson, D. W. Cryst. Growth Des. 2010, 10, 3531-3536
15. Biscarini, P.; Fusina, L.; Nivellini, G. D. Inorg. Chem. 1971, 10, 2564-2566
16. Sheldrick, G. M. Bruker/Siemens Area Detector Absorption Correction Program; Bruker AXS: Madison, WI, 1998.
17. Van der Sluis, P.; Spek, A. L. Acta Crystallogr., Sect. A 1990, A46, 194-201
18. SHELXTL-6.10 Program for Structure Solution, Refinement and Presentation; Bruker AXS Inc.: Madison, WI.
19. Zhang, P.; Bundle, D. R. Isr. J. Chem. 2000, 40, 189-208
20. Kader, A. T.; Stirling, C. J. M. J. Chem. Soc. 1962, 3425-3428
21. Autenrieth, W.; Beuttel, F. Ber. Dtsch. Chem. Ges. 1910, 42, 4346-57
22. Meyer, E. A.; Castellano, R. K.; Diederich, F. Angew. Chem., Int. Ed. 2003, 42, 1210-1250
23. Using the normalized distance function R HX = d (H•••Cl)/ (r H + r X) established in Brammer, L.; Bruton, E. A.; Sherwood, P. Cryst. Growth Des. 2001, 1, 277-290 the normalized H•••Cl distance for this compound (1.01) falls within the range of previously observed C-H•••Cl-M hydrogen bonds (C-H•••Cl angle = 145°)
24. Liu, C.-B.; Che, G.-B.; Cui, Y.-C.; Li, C.-B. Acta Crystallogr. 2005, E61, m2469-m2470
25. Yu, Q.; Tao, Y.; Li, J.-R. Acta Crystallogr. 2006, E62, m613-m614
26. Bharara, M. S.; Bui, T. H.; Parkin, S.; Atwood, D. A. Inorg. Chem. 2005, 44, 5753-5760
27. Krauter, G.; Neumuller, B.; Goedken, V. L.; Rees, W. S., Jr. Chem. Mater. 1996, 8, 360-368
28. Ramirez, J.; Stadler, A.-M.; Harrowfield, J. M.; Brelot, L.; Huuskonen, J.; Rissanen, K.; Allouche, L.; Lehn, J.-M. Z. Anorg. Allg. Chem. 2007, 633, 2435-2444
29. Zhou, H.-P.; Tian, Y.-P.; Wu, J.-Y.; Zhang, J.-Z.; Li, D.-M.; Zhu, Y.-M.; Hu, Z-J; Tao, X.-T.; Jiang, M.-H.; Xie, Y. Eur. J. Inorg. Chem. 2005, 4976-4984
30. Burchell, T. J; Eisler, D. J.; Puddephatt, R. J. Inorg. Chem. 2004, 43, 5550-5557