Trimer (chemistry)
In chemistry, a trimer (Template:IPAc-en; Template:Ety) is a molecule or polyatomic anion formed by combination or association of three molecules or ions of the same substance. In technical jargon, a trimer is a kind of oligomer derived from three identical precursors often in competition with polymerization.
Examples
Alkyne trimerization
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In 1866, Marcellin Berthelot reported the first example of cyclotrimerization, the conversion of acetylene to benzene.[1] This process was commercialized:
Nitrile trimerization
Symmetrical 1,3,5-triazines are prepared by trimerization of certain nitriles such as cyanogen chloride.
Cyanogen chloride and cyanogen bromide each trimerize at elevated temperatures over a carbon catalyst.[1] The chloride gives cyanuric chloride:
The bromide has an extended shelflife when refrigerated. Like the chloride, it undergoes ab exothermic trimerization to form cyanuric bromide. This reaction is catalyzed by traces of bromine, metal salts, acids and bases.[2] For this reason, experimentalists avoid brownish samples.[3]
An industrial route to cyanuric acid entails the thermal decomposition of urea, with release of ammonia. The conversion commences at approximately 175 °C:[4]
The endothermic synthesis of melamine can be understood in two steps.
First, urea decomposes into cyanic acid and ammonia in an endothermic reaction:
Then in the second step, cyanic acid polymerizes to form cyanuric acid, which condenses with the liberated ammonia from the first step to release melamine and water.
This water then reacts with cyanic acid present, which helps drive the trimerization reaction, generating carbon dioxide and ammonia.
In total, the second step is exothermic:
but the overall process is endothermic.
Diene trimerization
The 1,5,9-trans-trans-cis isomer of cyclododecatriene, which has some industrial importance is obtained by cyclotrimerization of butadiene with titanium tetrachloride and an organoaluminium co-catalyst:[5]
Breaking carbon-hetero double bonds forms symmetrical saturated 1,3,5-heterocycles
Cyclotrimerization of formaldehyde affords 1,3,5-Trioxane:
1,3,5-Trithiane is the cyclic trimer of the otherwise unstable species thioformaldehyde. This heterocycle consists of a six-membered ring with alternating methylene bridges and thioether groups. It is prepared by treatment of formaldehyde with hydrogen sulfide.[6]
Three molecules of acetaldehyde condense to form paraldehyde, a cyclic trimer containing C-O single bonds.
Catalyzing and dehydrating by sulfuric acid, trimerization of acetone via aldol condensation affords mesitylene[7]
Trisiloxanes
Dimethylsilanediol dehydrates to a trimer of Template:Chem2 as well as polydimethylsiloxane. The reaction illustrates the competition between trimerization and polymerization. The polymer and trimer are formally derived from the hypothetical sila-ketone Template:Chem2, although this species is not an intermediate.
Coordination chemistry
The dithiobenzoate complexes Template:Chem2 crystallize as trimers (M = Ni, Pd).[8]
See also
References
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- ↑ a b Script error: No such module "citation/CS1".
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- ↑ Klaus Huthmacher, Dieter Most "Cyanuric Acid and Cyanuric Chloride" Ullmann's Encyclopedia of Industrial Chemistry" 2005, Wiley-VCH, Weinheim. doi 10.1002/14356007.a08 191
- ↑ Industrial Organic Chemistry, Klaus Weissermel, Hans-Jurgen Arpe John Wiley & Sons; 3rd 1997 Template:ISBN
- ↑ Bost, R. W.; Constable, E. W. "sym-Trithiane" Organic Syntheses, Collected Volume 2, p.610 (1943). Script error: No such module "citation/CS1".
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