1945
DOI: 10.1021/ja01227a030
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Pyrolysis of Some Polyethylene Amines

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Cited by 7 publications
(5 citation statements)
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“…This suggests that the reaction conditions have resulted in cyclization of the TETN, leading to in situ formation of the effective templating agent piperazine. Decomposition of TETN to ethylenediamine and cyclized species has been reported to occur under conditions similar to those employed in synthesis here. Parise and Ko have observed similar cyclization of TETN at long reaction times during the synthesis of [C 4 H 8 N 2 ][Sb 4 S 7 ] .…”
Section: Resultsmentioning
confidence: 69%
“…This suggests that the reaction conditions have resulted in cyclization of the TETN, leading to in situ formation of the effective templating agent piperazine. Decomposition of TETN to ethylenediamine and cyclized species has been reported to occur under conditions similar to those employed in synthesis here. Parise and Ko have observed similar cyclization of TETN at long reaction times during the synthesis of [C 4 H 8 N 2 ][Sb 4 S 7 ] .…”
Section: Resultsmentioning
confidence: 69%
“…By controlling the temperature, two new organic-inorganic hybrid compounds, triethylenetetraammonium hexachloridostannate(IV) dichloride dihydrate, (C 6 Commercial triethylenetetramine is a mixture of linear TETA (typically 60%) and other branched or cyclic TETA, with close boiling points, such as tris-(2-aminoethyl)amine), 1,4-bis(2-aminoethyl)piperazine, (Bis AEP), and N-[(2aminoethyl)2-aminoethyl]piperazine). Piperazine derivatives are relatively more volatile than the corresponding linear polyethylene amines (Hutchinson et al, 1945).…”
Section: Chemical Contextmentioning
confidence: 99%
“…The principal types of organic species used are linear and branched long-chain aliphatic amines and polyamines and alicyclic amines. Long-chain polyamines, in particular, are frequently unstable at elevated temperatures . For example, under solvothermal conditions they can undergo side-reactions such as cyclization 3,15 and cleavage, thereby introducing further geometric diversity into the structure-directing agent.…”
Section: Introductionmentioning
confidence: 99%
“…Long-chain polyamines, in particular, are frequently unstable at elevated temperatures. 14 For example, under solvothermal conditions they can undergo sidereactions such as cyclization 3,15 and cleavage, 16 thereby introducing further geometric diversity into the structuredirecting agent. The products of such reactions consist of complex anionic metal-sulfide frameworks with protonated amines fulfilling the charge-balancing role.…”
Section: Introductionmentioning
confidence: 99%