homolytic dissociation of the vulcanization accelerator

Homolytic Dissociation of the Vulcanization Accelerator

The homolytic dissociation of the important vulcanization accelerator tetramethylthiuram disulfide (TMTD) has been studied by ab initio calculations according to the G3X(MP2) and G3X(MP2)-RAD theories. Homolytic cleavage of the SS bond requires a low enthalpy of 150.0 kJ mol-1, whereas 268.0 kJ mol-1 is needed for the dissociation of one of the C?S single bonds. To cleave one of the SS bonds

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Homolytic dissociation of the vulcanization accelerator

Steudel, R., Steudel, Y., Mak, A.M., Ming, W.W. (2006-12-08). Homolytic dissociation of the vulcanization accelerator tetramethylthiuram disulfide (TMTD) and structures and stabilities of the related radicals Me 2NCSn ? (n = 1-4). Journal of Organic Chemistry 71 (25) : 9302-9311. ScholarBank@NUS Repository. https://doi.org/10.1021/jo061345o

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Homolytic S-S bond dissociation of 11 bis(thiocarbonyl

Homolytic dissociation of the vulcanization accelerator tetramethylthiuram disulfide (TMTD) and structures and stabilities of the related radicals Me 2 NCS n (n = 1-4) Author STEUDEL, Ralf 1 ; STEUDEL, Yana 1 ; MATTHEW MAK, Adrian 2 ; MING WAH WONG 2 [1] Institut für Chemie, Technische Universit?t Berlin, Sekr.

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Homolytic dissociation of the vulcanization accelerator

The homolytic dissociation of the important vulcanization accelerator tetramethylthiuram disulfide (TMTD) has been studied by ab initio calculations according to the G3X(MP2) and G3X(MP2)-RAD theories.

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Homolytic S-S Bond Dissociation of 11 Bis(thiocarbonyl

Homolytic S S Bond Dissociation of 11 Bis (thiocarbonyl)disulfides R‐C ( S) S S C ( S)R and Prediction of A Novel Rubber Vulcanization Accelerator - Mak - 2008 - Chemistry – An Asian Journal - Wiley Online Library.

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Homolytic dissociation of the vulcanization accelerator

Homolytic dissociation of the vulcanization accelerator tetramethylthiuram disulfide (TMTD) and structures and stabilities of the related radicals Me 2NCSn ? (n = 1-4). Journal of Organic Chemistry 71 (25) : 9302-9311.

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Homolytic dissociation of the vulcanization accelerator

Homolytic Dissociation of the Vulcanization Accelerator Tetramethylthiuram Disulfide (TMTD) and Structures and Stabilities of the Related Radicals Me 2 NCS n ? ( n = 1?4). The Journal of Organic Chemistry 2006 , 71 (25) , 9302-9311.

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PRIME PubMed | Homolytic dissociation of the vulcanization

The homolytic dissociation of the important vulcanization accelerator tetramethylthiuram disulfide (TMTD) has been studied by ab initio calculations according to the G3X(MP2) and G3X(MP2)-RAD theories. Homolytic cleavage of the SS bond requires a low enthalpy of 150.0 kJ mol-1, whereas 268.0 kJ mol-1 is needed for the dissociation of one of the C-S single bonds. To cleave one of the SS bonds

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Homolytic dissociation of the vulcanization accelerator

Homolytic dissociation of the vulcanization accelerator tetramethylthiuram disulfide (TMTD) and structures and stabilities of the related radicals Me 2 NCS n (n = 1-4) Author STEUDEL, Ralf 1; STEUDEL, Yana 1; MATTHEW MAK, Adrian 2; MING WAH WONG 2 [1] Institut für Chemie, Technische Universit?t Berlin, Sekr.

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Homolytic Dissociation of the Vulcanization Accelerator

The homolytic dissociation of the important vulcanization accelerator tetramethylthiuram disulfide (TMTD) has been studied by ab initio calculations according to the G3X(MP2) and G3X(MP2)-RAD theories. Homolytic cleavage of the SS bond requires a low enthalpy of 150.0 kJ mol-1, whereas 268.0 kJ mol-1 is needed for the dissociation of one of the C?S single bonds. To cleave one of the SS bonds

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Staff View: Homolytic dissociation of the vulcanization

Homolytic dissociation of the vulcanization accelerator tetramethylthiuram disulfide (TMTD) and structures and stabilities of the related radicals Me 2NCSn ? (n = 1-4). Journal of Organic Chemistry 71 (25) : 9302-9311.

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Recent Advances on the Polymerization of Elemental Sulphur

vulcanization process are discussed. 2.1.1 Revisiting the homolytic ROP of S. 8. The phase transitions and behaviour of the allotropes of sulfur have been extensively discussed. 30, 33-36. The thermody-namically stable form of sulfur is orthorhombic sulfur, usually designated as α-S. 8, which is reported to convert to the mono-clinic β-S. 8

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Homolytic S-S bond dissociation of 11 bis(thiocarbonyl

Bis(thiocarbonyl)disulfide with a guanidine-type substituent, (Gu(1)CS(2))(2), is predicted to be an effective accelerator in sulfur vulcanization of rubber. Compared to TMTD, (Gu(1)CS(2))(2) is calculated to have a lower bond dissociation enthalpy and smaller associated barrier for the S-S homolysis.

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Water‐Assisted Homolytic Dissociation of Propyne on a Reduced

DC Field Value; dc.title: Homolytic SS bond dissociation of 11 bis(thiocarbonyl)disulfides R-C(=S)-S-S-C(=S)R and prediction of A novel rubber vulcanization accelerator

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