Structure of D-ribonic acid-dimethyltin(IV) in coordinating solvents: An experimental and DFT119Sn NMR study

Journal of Physical Organic Chemistry

Volumn 19, Issue 12, 2006, Pages 874-883

  Bagno, Alessandro ^a   Bertazzi, Nuccio ^b   Casella, Girolamo ^b   Pellerito, Lorenzo ^b   Saielli, Giacomo ^c   Sciacca, Ivan D ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b UNIVERSITY OF PALERMO   (Italy)

^c INSTITUTE ON MEMBRANE TECHNOLOGY   (Italy)

Author keywords

119Sn NMR; Carbohydrate metal complexes; DFT calculations; Organotin compounds; Ribonic acid

Indexed keywords

CONFORMATIONS; DENSITY FUNCTIONAL THEORY; DIMERIZATION; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

CARBOHYDRATE-METAL COMPLEXES; COORDINATING SOLVENTS; ORGANOTIN COMPOUNDS; RIBONIC ACID;

ORGANIC ACIDS;

EID: 33947155408     PISSN: 08943230     EISSN: 10991395     Source Type: Journal    
DOI: 10.1002/poc.1041     Document Type: Article

References (40)

1. Jousseame B, Pereyre M. In Chemistry of Tin, Smith PJ (ed.). Chapman & Hall: London, 1998.
2. Evans CJ. In Chemistry of Tin, Smith PJ (ed.). Chapman & Hall: London, 1998.
3. David S, Hanessian S. Tetrahedron 1985; 41: 643-663. DOI: 10.1016/S0040-4020(01)86443-9
4. Grindley TB. Adv. Carbodr. Chem. 1998; 53: 17-142.
5. Arakawa Y. In Chemistry of Tin, Smith PJ (ed.). Chapman & Hall: London, 1998.
6. Saxena AK, Huber F. Coord. Chem. Rev. 1989; 95:109-123. DOI: 10.1016/0010-8545(89)80003-7
7. Tsangaris JM, Williams DR. Appl. Organomet. Chem. 1992; 6: 3-18.
8. Gielen M. Appl. Organomet. Chem. 2002; 16: 481-494. DOI: 10.1002/aoc.331
9. Whitfield DM, Stojkovski S, Sarkar B. Coord. Chem. Rev. 1993; 122: 171-225. DOI: 10.1016/0010-8545(93)80045-7
10. Gyurcsik B, Nagy L. Coord. Chem. Rev. 2000; 203: 81-149. DOI: 10.1016/S0010-8545(99)00183-6
11. Petrou AL. Coord. Chem. Rev. 2002; 228: 153-162.
12. Pellerito L, Nagy L. Coord. Chem. Rev. 2002; 224: 111-150 and references therein. DOI: 10.1016/S0010-8545(01)00399-X
13. Bertazzi N, Bruschetta G, Casella G, Pellerito L, Rotondo E, Scopelliti M. Appl. Organomet. Chem. 2003; 17: 932-939. DOI: 10.1002/aoc.556
14. Smith PJ, Tupčiauskas AP. Ann. Rep. NMR Spectrosc. 1978; 8: 291-370.
15. Hani R, Geanagel RA. Coord. Chem. Rev. 1982; 44: 229-246. DOI: 10.1016/S0010-8545(00)80522-6
16. Wrackmeyer B. Ann. Rep. NMR Spectrosc. 1985; 16: 73-186.
17. Wrackmeyer B. Ann. Rep. NMR Spectrosc. 1999; 38: 203-264.
18. Nakatsuji H, Inoue T, Nakao T. J. Phys. Chem. 1992; 96: 7953-7958. DOI: 10.1021/J100199A025
19. Vivas-Reyes R, De Proft F, Biesemans M, Willem R, Geerlings P. J. Phys. Chem. A 2002; 106:2753-2759. DOI: 10.1021/JP0145917
20. Kaneko H, Hada M, Nakajima T, Nakatsuji H. Chem. Phys. Lett. 1996; 261: 1-6. DOI: 10.1016/0009-2614(96)00906-2
21. Avalle P, Harris RK, Fischer RD. Phys. Chem. Chem. Phys. 2002; 4: 3558-3561. DOI:10.1039/B202909J
22. Avalle P, Harris RK, Kardakov PB, Wilson PJ. Phys. Chem. Chem. Phys. 2002; 4: 5925-5932. DOI:10.1039/B208435J
23. Kirpekar S, Jensen HJA, Oddershede J. Theor. Chim. Acta 1997; 95: 35-47. DOI: 10.1007/s002140050181
24. Enevoldsen T, Visscher L, Saue T, Jensen HJA, Oddershede J. J. Chem: Phys. 2000; 112: 3493-3498. DOI: 10.1063/1.480504
25. Khandogin J, Ziegler T. J. Phys. Chem. A 2000; 104: 113-120. DOI: 10.1021/JP992571N
26. Bagno A, Casella G, Saielli G. J. Chem. Theory Comput. 2006; 2: 37-46. DOI: 10.1021/ct050173k
27. Bath KL, Chen SY, Joullié MM. Heterocycles 1985; 23: 691-729.
28. Matzanke BF, Böhnke R, Bill E, Trautwein AX, Winkler H. J. Inorg. Biochem. 1995; 59: 111-111.
29. Yu RJ, Van Scott EJ, Aug 1997, U.S. Pat. N. 5,583,156.
30. Yu RJ, Van Scott EJ, Aug 1997, U.S. Pat. N. 5,656,666.
31. Becke AD. J. Chem. Phys. 1993; 98: 5648-5652.
32. Perdew JP, Chevary JA, Vosko SH, Jackson KA, Pederson MR, Singh DJ, Fiolhais C. Phys. Rev. B 1992; 46: 6671-6687.
33. Lee C, Yang W, Parr RG. Phys. Rev. B 1988; 37: 785-789.
34. Kutzelnigg W, Fleischer U, Schindler M. In NMR Basic Principles and Progress, Diehl P, Fluck E, Günther H, Kosfeld R, Seelig J (eds). Springer-Verlag: Heidelberg, 1991.
35. Gaussian 98, Revision A.9, Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Zakrzewski VG, Montgomery JA Jr., Stratmann RE, Burant JC, Dapprich S, Millam JM, Daniels AD, Kudin KN, Strain MC, Farkas O, Tomasi J, Barone V, Cossi M, Cammi R, Mennucci B, Pomelli C, Adamo C, Clifford S, Ochterski J, Petersson GA, Ayala PY, Cui Q, Morokuma K, Malick DK, Rabuck AD, Raghavachari K, Foresman JB, Cioslowski J, Ortiz JV, Baboul AG, Stefanov BB, Liu G, Liashenko A, Piskorz P, Komaromi I, Gomperts R, Martin RL, Fox DJ, Keith T, Al-Laham MA, Peng CY, Nanayakkara A, Challacombe M, Gill PMW, Johnson B, Chen W, Wong MW, Andres JL, Gonzalez C, Head-Gordon M, Replogle ES, Pople JA, Gaussian, Inc., Pittsburgh PA, 1998.
36. Lockhart TP, Manders WF. Inorg. Chem. 1986; 25: 892-895. DOI:10.1021/ic00227a002
37. Haasnoot CAG, dew Leeuw FAAM, Altona C. Tetrahedron 1980; 36: 2783-2792. DOI:10.1016/0040-4020(80)80155-4
38. Karplus M. J. Phys. Chem. 1959; 30: 11-15.
39. Karplus M. J. Am. Chem. Soc. 1963; 85: 2870-2871.
40. Huggins ML. J. Am. Chem. Soc. 1953; 75: 4123-4126.