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- [[Category:Aromatic amines]]4 KB (634 words) - 13:12, 20 September 2010
- [[Category:Aromatic amines]]3 KB (435 words) - 13:12, 20 September 2010
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- ...y amine]]; by the condensation of ''para''-aminoazo compounds with primary amines, and by the action of ''para''-nitrosodialkylanilines with secondary [[base [[Category:Aromatic amines]]5 KB (638 words) - 13:12, 20 September 2010
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- [[Category:aromatic amines]]2 KB (276 words) - 13:12, 20 September 2010
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- [[Category:Aromatic amines]]21 KB (3,043 words) - 13:13, 20 September 2010
- [[Category:Aromatic amines|Naphthylamine, 1-]]3 KB (399 words) - 13:13, 20 September 2010
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- [[Category:Aromatic amines]]15 KB (1,980 words) - 13:13, 20 September 2010
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- ===Adding ammonia and amines=== Similarly proceed the reactions with primary and secondary amines:82 KB (11,709 words) - 21:31, 20 September 2010
- ...tical workers (drugs, enzymes), seafood processors, shellac handlers (e.g. amines), solderers and refiners (metals), spray painters, insulation installers, p26 KB (3,697 words) - 21:31, 20 September 2010
- ...Kadlubar FF, Kulldorff M, ''et al.'' |title=Dietary intake of heterocyclic amines and benzo(a)pyrene: associations with pancreatic cancer |journal=Cancer Epi94 KB (13,321 words) - 21:32, 20 September 2010
- .... Hydrogen-bonds are formed between the three hydrogen atoms of protonated amines and three oxygen atoms of 18-crown-6. These hydrogen-bonds make the complex6 KB (864 words) - 20:14, 21 September 2010
- [[Category:Amines]]2 KB (302 words) - 20:14, 21 September 2010
- [[Category:Amines]]4 KB (504 words) - 20:14, 21 September 2010
- [[Category:Amines]]5 KB (728 words) - 20:14, 21 September 2010
- ...me=Ullmann>Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-V ...ldehyde]]s and [[ketone]]s. Because of its bifunctional nature, having two amines, it readily forms heterocycles such as [[imidazolidine]]s. Ethylenediamine9 KB (1,089 words) - 20:14, 21 September 2010
- [[Category:Amines]]4 KB (531 words) - 20:15, 21 September 2010
- [[Category:Amines]]2 KB (215 words) - 20:15, 21 September 2010
- Other [[dithiocarbamate]]s can be prepared similarly from secondary amines and carbon disulfide. They are used as [[chelating agents]] for transition5 KB (586 words) - 20:15, 21 September 2010
- ...It is soluble in polar solvents and exhibits the reactivity of typical for amines. The branched [[isomer]] N(CH<sub>2</sub>CH<sub>2</sub>NH<sub>2</sub>)<sub ...me=Ullmann>Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-V3 KB (369 words) - 20:15, 21 September 2010
- *Precursor to related imino ligands: Acetylacetone condenses with amines to give, successively, the mono- and the di-[[diketimine]]s wherein the O a16 KB (2,268 words) - 20:15, 21 September 2010
- [[Category:Amines]]2 KB (202 words) - 20:15, 21 September 2010
- [[Category:Amines]]10 KB (1,372 words) - 20:15, 21 September 2010
- ...igands. EDTA<sup>4-</sup> usually binds to a metal cation through its two amines and four carboxylates. Many of the resulting [[complex (chemistry)|coordin [[Category:Amines]]21 KB (3,011 words) - 16:51, 27 September 2010
- * Very lipophilic amines that do not easily dissolve in the aqueous phase in their charged form, e.g * Lower amines like [[ammonia]], [[methylamine]], or [[triethanolamine]] which are miscibl5 KB (812 words) - 20:16, 21 September 2010
- ...]], but Pd<sup>2+</sup> forms stronger complexes with phosphines than with amines. Later, Pearson proposed the theory of [[HSAB theory|hard and soft acids an50 KB (7,450 words) - 20:16, 21 September 2010
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- Virtually all ligands are known to bridge, with the exception of amines and ammonia.<ref>{{cite journal | last = Werner | first = H. | year = 20044 KB (576 words) - 20:18, 21 September 2010
- ...-David, Y. and Milstein, D., "Direct Synthesis of Amides from Alcohols and Amines with Liberation of H<sub>2</sub>", Science, 2007, 317, 790-792.{{doi|10.1125 KB (747 words) - 20:18, 21 September 2010
- ...wiki></sup>, when it is sexidentate, binds as a κ<sup>6</sup>-ligand, the amines and the carboxylate oxygen atoms are not contiguous. In practice, the n val25 KB (3,607 words) - 20:18, 21 September 2010
- [[Category:Amines]]4 KB (584 words) - 20:18, 21 September 2010
- ...singlet ground-state; that is, they have lone electron pairs (e.g. water, amines, ethers), so these substrates need an empty orbital to be able to react wit25 KB (3,677 words) - 20:18, 21 September 2010
- ...f coordination compounds. Octahedral transition-metal complexes containing amines and simple anions are often referred to Werner-type complexes.10 KB (1,633 words) - 20:18, 21 September 2010
- [[Category:Aromatic amines]]2 KB (284 words) - 21:29, 21 September 2010
- [[Category:Biogenic amines]]2 KB (267 words) - 22:12, 21 September 2010
- [[Category:Amines]]61 KB (8,865 words) - 22:13, 21 September 2010
- [[Category:Amines]]2 KB (268 words) - 22:15, 21 September 2010
- [[Category:Amines]]2 KB (209 words) - 22:15, 21 September 2010
- [[Category:Aromatic amines]]28 KB (3,886 words) - 22:16, 21 September 2010
- ...[tyramine]]. Some aged cheeses contain significant concentrations of these amines, which can trigger symptoms mimicking an [[allergic reaction]]: [[headache]51 KB (7,545 words) - 19:38, 13 October 2010
- ...Kerstin Skog, Håkan Olsson, Elisabet Wirfält |title=Do both heterocyclic amines and omega-6 polyunsaturated fatty acids contribute to the incidence of brea32 KB (4,810 words) - 19:39, 13 October 2010