1996
DOI: 10.1016/0277-5387(95)00340-1
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The chemistry of inorganic and organometallic compounds with adamantane-like structures

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Cited by 45 publications
(41 citation statements)
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“…Memantine and amantadine are derivatives of the cycloalkane, adamantane (which makes up the 10 carbon cage-like backbone in both compounds). Methenamine is an adamantane analogue, and in this, the cage-like backbone includes seven carbons and three nitrogens 9. In healthy subjects, amantadine results in an increase in circulating norepinephrine, and a decrease in epinephrine, dopamine and serotonin 10.…”
Section: Discussionmentioning
confidence: 99%
“…Memantine and amantadine are derivatives of the cycloalkane, adamantane (which makes up the 10 carbon cage-like backbone in both compounds). Methenamine is an adamantane analogue, and in this, the cage-like backbone includes seven carbons and three nitrogens 9. In healthy subjects, amantadine results in an increase in circulating norepinephrine, and a decrease in epinephrine, dopamine and serotonin 10.…”
Section: Discussionmentioning
confidence: 99%
“…It is known that oxidative addition of the Sn(IV)-E bonds in the ring compounds [(R 2 SnE) 3 ] (R = Me, Ph) to complex 1 occurs easily, giving interesting platinum(IV) complexes containing PtESnESn rings (3). By analogy, it was considered possible that oxidative addition of the Hg(II)-E bonds of the adamantanoid compounds [Hg 4 (EPh) 6 (L) 4 ][ClO 4 ] 2 (2a-d) (Chart 1), might give novel cage complexes containing platinum(IV) centres (4,5).…”
Section: Introductionmentioning
confidence: 99%
“…No 1:1 cationic complex has so far been crystallographically characterised. [11] The adamantane-like tetrahedral cage M 4 (µ-S) 6 , which is the most frequently encountered structural unit in polynuclear thiolates, [12,13] is also present in cationic thioamide complexes. This tetrahedral cage is known to exist, with no terminal ligands and thus with trigonal coordination of all four metal atoms, in [Cu 4 L 6 ] 4ϩ species [L ϭ tu (thiourea), [14,15] thpym2tH 2 (tetrahydropyrimidine-2-thione), [16] and with the accommodation of some terminal ligands and both tetrahedral and trigonal metal sites in complexes [Cu 4 -(tu) 7 ](SO 4 ) 2 , [17] [Cu 4 (tu) 9 ](NO 3 ) 4 , [18] and [{Cu 4 (tu) 6 (tu) 3/2 } (SO 4 ) 2 ] n .…”
Section: Introductionmentioning
confidence: 99%
“…[44] The chemical shifts of these [8.90 (1), 14.10 (2) ppm], as well as their positive coordination shifts, reflect, as in the IR spectra, the relevant contribution of the immonium-thiolate resonance form in both complexes. 13 C NMR spectra are more sensitive to S-donation, the carbon atom of the thione group being the most affected, with high-field coordination shifts [45,46] of δ ϭ Ϫ5.2 and Ϫ10.2 ppm, respectively, for complexes 1 and 2.…”
mentioning
confidence: 98%