메뉴 건너뛰기




Volumn 40, Issue 17, 2011, Pages 4505-4513

Oxidative properties of iodine-adducts of propylthiouracil and methimazole: Direct synthesis of mercury(ii) complexes from the reaction with liquid mercury

Author keywords

[No Author keywords available]

Indexed keywords

CHARGE SEPARATIONS; COMPLEXING PROPERTIES; CRYSTAL PACKINGS; DIRECT SYNTHESIS; GOOD YIELD; INTERMOLECULAR HYDROGEN BONDS; IODINE ATOMS; LINEAR MOLECULES; LIQUID MERCURY; MERCURY COMPLEX; METHIMAZOLE; NEUTRAL COMPLEXES; OXIDATIVE ADDITIONS; OXIDATIVE PROPERTIES; SINGLE CRYSTAL X-RAY DIFFRACTION ANALYSIS; SULFUR ATOMS; TETRAETHYLAMMONIUM; TETRAHEDRAL GEOMETRY; TWO-ELECTRON TRANSFER; WASTE ELECTRICAL AND ELECTRONIC EQUIPMENT;

EID: 79954602847     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/c0dt01409e     Document Type: Article
Times cited : (30)

References (32)
  • 2
    • 34250827959 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 8
    • 84945025752 scopus 로고
    • 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 scopus 로고
    • 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
  • 16
    • 0038667549 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.