-
2
-
-
34250827959
-
-
11/ed, Chapter 65, L. L. Brunton, J. S. Lazo, K. L. Parker), The McGraw-Hill Companies, Inc. USA, 1753-1776
-
C. D. Klaassen, Goodman & Gilman's the Pharmacological Basis of Therapeutics, 11/ed, Chapter 65 (Eds:, L. L. Brunton, J. S. Lazo, K. L. Parker,), The McGraw-Hill Companies, Inc. USA, 2006, pp. 1753-1776
-
(2006)
Goodman & Gilman's the Pharmacological Basis of Therapeutics
-
-
Klaassen, C.D.1
-
3
-
-
36248976131
-
-
eds. P. Metrangolo and G. Resnati) Spinger-Verlag, Berlin, and references therein
-
2 to give 1:1 adducts containing an almost linear S-I-I fragment can be seen as a charge-transfer process. It occurs via the transfer of charge density from a lone pair of electrons (n) on the donor atom to the empty σ* antibonding orbital of the iodine species. Depending on the charge density transferred by the DS donor molecule and solvent nature, this can result in lengthening of the I-I bond length up to breaking of the bond. W. T. Pennington, T. W. Hanks, H. D. Arman, Halogen Bonding: Fundamentals and Applications, (Eds:, P. Metrangolo, and, G. Resnati,) Spinger-Verlag, Berlin 2008, pp. 65-104, and references therein
-
(2008)
Halogen Bonding: Fundamentals and Applications
, pp. 65-104
-
-
Pennington, W.T.1
Hanks, T.W.2
Arman, H.D.3
-
4
-
-
79954627586
-
-
F. A. Devillanova), RCS Publishing: Cambridge, U. K 477-496
-
V. Lippolis, F. Isaia, Handbook of Chalcogen Chemistry, Chapter 8.2, (Ed., F. A. Devillanova,), RCS Publishing: Cambridge, U. K 2007; pp. 477-496
-
(2007)
Handbook of Chalcogen Chemistry, Chapter 8.2, (Ed.
-
-
Lippolis, V.1
Isaia, F.2
-
5
-
-
11144304622
-
-
M. C. Aragoni M. Arca M. B. Carrea F. Demartin F. A. Devillanova A. Garau F. Isaia V. Lippolis G. Verani Eur. J. Inorg. Chem. 2004 23 4660 4668
-
(2004)
Eur. J. Inorg. Chem.
, vol.23
, pp. 4660-4668
-
-
Aragoni, M.C.1
Arca, M.2
Carrea, M.B.3
Demartin, F.4
Devillanova, F.A.5
Garau, A.6
Isaia, F.7
Lippolis, V.8
Verani, G.9
-
8
-
-
84945025752
-
-
Notwithstanding the hydrogen atoms of the methanol were not included in the refinement, the orientation of the molecule and the distance of 3.61 Å between the O and the I2 atoms are congruent with the presence of a hydrogen bond
-
P. D. Cookson E. R. T. Tiekink Z. Kristallogr. 1994 209 749 751
-
(1994)
Z. Kristallogr.
, vol.209
, pp. 749-751
-
-
Cookson, P.D.1
Tiekink, E.R.T.2
-
10
-
-
33748842545
-
-
2 salt-inclusion compound.
-
M. C. Etter J. Phys. Chem. 1991 95 4601 4610
-
(1991)
J. Phys. Chem.
, vol.95
, pp. 4601-4610
-
-
Etter, M.C.1
-
15
-
-
46849117789
-
-
F. Isaia M. C. Aragoni M. Arca F. Demartin F. A. Devillanova G. Floris A. Garau M. B. Hursthouse V. Lippolis R. Medda F. Oppo M. Pira G. Verani J. Med. Chem. 2008 51 4050 4053
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4050-4053
-
-
Isaia, F.1
Aragoni, M.C.2
Arca, M.3
Demartin, F.4
Devillanova, F.A.5
Floris, G.6
Garau, A.7
Hursthouse, M.B.8
Lippolis, V.9
Medda, R.10
Oppo, F.11
Pira, M.12
Verani, G.13
-
16
-
-
0038667549
-
-
2-adducts, it is possible to classify the adducts into three categories: (i) weak adducts, d(I-I) < 2.86 Å, where the iodine molecule, is only slightly perturbed/lengthened by the donor molecule interaction; (ii) strong adducts, where the molecular entity I-I can still be recognized and featuring 2.86 Å < d(I-I) < 3.01 Å; (iii) very strong adducts, where the d(I-I) > 3.01 Å. See Reference 5
-
C. T. Antoniadis G. J. Corban S. K. Hadjikakou N. Hadjiliadis M. Kubicki S. Warner I. S. Butler Eur. J. Inorg. Chem. 2003 8 1635 1640
-
(2003)
Eur. J. Inorg. Chem.
, vol.8
, pp. 1635-1640
-
-
Antoniadis, C.T.1
Corban, G.J.2
Hadjikakou, S.K.3
Hadjiliadis, N.4
Kubicki, M.5
Warner, S.6
Butler, I.S.7
-
24
-
-
0242560405
-
-
A. Altomare M. C. Burla M. Camalli G. L. Cascarano C. Giacovazzo A. Guagliardi A. Moliterni G. Polidori R. Spagna J. Appl. Crystallogr. 1999 32 115 119
-
(1999)
J. Appl. Crystallogr.
, vol.32
, pp. 115-119
-
-
Altomare, A.1
Burla, M.C.2
Camalli, M.3
Cascarano, G.L.4
Giacovazzo, C.5
Guagliardi, A.6
Moliterni, A.7
Polidori, G.8
Spagna, R.9
-
27
-
-
0038626673
-
-
Gaussian, Inc., Wallingford CT
-
M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, and J. A. Pople, Gaussian 03, Gaussian, Inc., Wallingford CT, 2004
-
(2004)
Gaussian 03
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Montgomery Jr., J.A.7
Vreven, T.8
Kudin, K.N.9
Burant, J.C.10
Millam, J.M.11
Iyengar, S.S.12
Tomasi, J.13
Barone, V.14
Mennucci, B.15
Cossi, M.16
Scalmani, G.17
Rega, N.18
Petersson, G.A.19
Nakatsuji, H.20
Hada, M.21
Ehara, M.22
Toyota, K.23
Fukuda, R.24
Hasegawa, J.25
Ishida, M.26
Nakajima, T.27
Honda, Y.28
Kitao, O.29
Nakai, H.30
Klene, M.31
Li, X.32
Knox, J.E.33
Hratchian, H.P.34
Cross, J.B.35
Bakken, V.36
Adamo, C.37
Jaramillo, J.38
Gomperts, R.39
Stratmann, R.E.40
Yazyev, O.41
Austin, A.J.42
Cammi, R.43
Pomelli, C.44
Ochterski, J.W.45
Ayala, P.Y.46
Morokuma, K.47
Voth, G.A.48
Salvador, P.49
Dannenberg, J.J.50
Zakrzewski, V.G.51
Dapprich, S.52
Daniels, A.D.53
Strain, M.C.54
Farkas, O.55
Malick, D.K.56
Rabuck, A.D.57
Raghavachari, K.58
Foresman, J.B.59
Ortiz, J.V.60
Cui, Q.61
Baboul, A.G.62
Clifford, S.63
Cioslowski, J.64
Stefanov, B.B.65
Liu, G.66
Liashenko, A.67
Piskorz, P.68
Komaromi, I.69
Martin, R.L.70
Fox, D.J.71
Keith, T.72
Al-Laham, M.A.73
Peng, C.Y.74
Nanayakkara, A.75
Challacombe, M.76
Gill, P.M.W.77
Johnson, B.78
Chen, W.79
Wong, M.W.80
Gonzalez, C.81
Pople, J.A.82
more..
-
28
-
-
68549083563
-
-
F. Isaia M. C. Aragoni M. Arca F. Demartin F. A. Devillanova G. Ennas A. Garau V. Lippolis A. Mancini G. Verani Eur. J. Inorg. Chem. 2009 3667 3672
-
(2009)
Eur. J. Inorg. Chem.
, pp. 3667-3672
-
-
Isaia, F.1
Aragoni, M.C.2
Arca, M.3
Demartin, F.4
Devillanova, F.A.5
Ennas, G.6
Garau, A.7
Lippolis, V.8
Mancini, A.9
Verani, G.10
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