Condensation reactions of carbon disulfide

1969 ◽  
Vol 46 (12) ◽  
pp. 841 ◽  
Author(s):  
William O. Foye
Keyword(s):  
Carbon Disulfide ◽  
Condensation Reactions

Polyphenyl polysulfide: a new polymer cathode material for Li–S batteries

2019 ◽  
Vol 55 (33) ◽  
pp. 4857-4860 ◽  
Author(s):  
Pengfei Sang ◽  
Yubing Si ◽  
Yongzhu Fu
Keyword(s):  
Cathode Material ◽  
Carbon Disulfide ◽  
Room Temperature ◽  
Molar Ratios ◽  
New Class ◽  
Condensation Reactions

We report a new class of polyphenyl polysulfides synthesized by condensation reactions between 4,4′-thiobisbenzenethiol (TBBT) and sulfur with four different molar ratios in a toluene/carbon disulfide mixture at room temperature.

Improvement in the Fock test for determining the reactivity of dissolving pulp

TAPPI Journal ◽  
2013 ◽  
Vol 12 (11) ◽  
pp. 21-26 ◽  
Author(s):  
CHAO TIAN ◽  
LINQIANG ZHENG ◽  
QINGXIAN MIAO ◽  
CHRIS NASH ◽  
CHUNYU CAO ◽  
...  
Keyword(s):  
Moisture Content ◽  
Sodium Hydroxide ◽  
Constant Temperature ◽  
Carbon Disulfide ◽  
Testing Procedure ◽  
Dissolving Pulp ◽  
Water Bath ◽  
Testing Conditions ◽  
Pulp Sample ◽  
Fock Reactivity

The Fock test is widely used for assessing the reactivity of dissolving pulp. The objective of this study was to modify the method to improve the repeatability of the test. Various parameters that affect the repeatability of the Fock test were investigated. The results showed that Fock reactivity is dependent on testing conditions affecting the xanthation between cellulose and carbon disulfide, such as the moisture content of the pulp sample, sodium hydroxide (NaOH) concentration, xanthation temperature, carbon disulfide dosage, and xanthation time. The repeatability of the test was significantly improved using the following modified testing procedure: air dried sample in the constant temperature/humidity room, xanthation temperature of 66°F (19°C) in a water bath, xanthation time of 3 h, NaOH concentration of 9% (w/w), and 1.3 mL carbon disulfide.

Reactions of Carbon Disulfide and Carbon Dioxide Adducts (eta5-C5H5)(CO) 2Fe-CX2 with Organoiron Electrophiles

1988 ◽  
Author(s):  
Mary E. Giuseppetti ◽  
Bruce E. Landrum ◽  
John L. Shibley ◽  
Alan R. Cutler
Keyword(s):  
Carbon Dioxide ◽  
Carbon Disulfide

Knoevenagel Condensation Reactions of Cyano Malononitrile-Derivatives Under Microwave Radiation

2018 ◽  
Vol 22 (6) ◽  
pp. 519-532 ◽  
Author(s):  
Lucas Lima Zanin ◽  
David Esteban Quintero Jimenez ◽  
Luis Pina Fonseca ◽  
Andre Luiz Meleiro Porto
Keyword(s):  
Microwave Radiation ◽  
Knoevenagel Condensation ◽  
Condensation Reactions

Influence of Metal Core Composition on Redox Properties and Photoreactivity of the Clusters [H4-xRu4-xRhx(CO)12] (x = 0, 2, 3, 4)

2001 ◽  
Vol 66 (7) ◽  
pp. 1062-1077 ◽  
Author(s):  
Maarten J. Bakker ◽  
Tapani A. Pakkanen ◽  
František Hartl
Keyword(s):  
Electrochemical Properties ◽  
Electrochemical Reduction ◽  
Redox Properties ◽  
Metal Core ◽  
Loss Product ◽  
Condensation Reactions ◽  
Core Composition ◽  
Co Dissociation ◽  
Major Reduction

Electrochemical properties of tetrahedral clusters [H2Ru2Rh2(CO)12], [HRuRh3(CO)12] and [Rh4(CO)12] were investigated in order to evaluate the influence of metal core composition in the series [H4-xRu4-xRhx(CO)12] (x = 0-4). The cluster [H3Ru3Rh(CO)12] was not available in sufficient quantities. As reported for [H4Ru4(CO)12], electrochemical reduction of the hydride-containing clusters [H2Ru2Rh2(CO)12] and [HRuRh3(CO)12] also results in (stepwise) loss of hydrogen, producing the anions [HRu2Rh2(CO)12]-, [Ru2Rh2(CO)12]2- and [RuRh3(CO)12]-. These anions can also be prepared from the neutral parent clusters via chemical routes. Electrochemical reduction of [Rh4(CO)12] does not result in the formation of any stable tetranuclear anion. Instead, [Rh5(CO)15]- and [Rh6(CO)15]2- are the major reduction products detected in the course of IR spectroelectrochemical experiments. Most likely, these cluster species are formed from the secondary CO-loss product [Rh4(CO)11]2- by fast redox condensation reactions. Their reoxidation regenerates parent [Rh4(CO)12], together with some [Rh6(CO)16]. Unlike [H4Ru4(CO)12] that undergoes photochemical CO-dissociation, [H2Ru2Rh2(CO)12] and [Rh4(CO)12] are completely photostable in neat hexane and dichloromethane as well as in the presence of oct-1-ene.

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