نتایج جستجو برای: thiocyanates
تعداد نتایج: 807 فیلتر نتایج به سال:
where Ws and WL represent the number of independent ways of realizing the arrangements of solid and melt respectively and Sf is the entropy of fusion. Each new kind of disorder which occurs on passing from the crystal to the melt involves a new mechanism of randomization on melting. Ubbelohde! has summarized the different ways of randomization in the transition from the solid to the melt as pos...
The copper-catalyzed cyanation of disulfides by azobisisobutyronitrile (AIBN) was developed, leading to thiocyanates in moderate to good yields. This procedure tolerates a series of functional groups, such as chloro, nitro, methyl and methoxycarbonyl in the phenyl ring of disulfides. Notably, it enables the use of two ArS units in (ArS)2. CuI was found to be essential for the in situ formation ...
This review highlights structural and biosynthetic work on a group of nitrogen-functionalised terpenes that are almost exclusively found in marine invertebrates and the animals that feed on them. The chemical functionality reviewed includes isocyanides, isothiocyanates, formamides, thiocyanates, isocyanates, and dichloroimines. The literature through mid 2003 is reviewed and there are 143 citat...
Given the severity of the complications of thyroid disorders, discussed in the work of Migneco et al1, we questioned if a dietotherapy approach could prevent acute events and chronic conditions. Thyroid-related metabolic disorders are numerous. Often, their exacerbation, as hyperthyroidism, can cause states of organic decompensation up to real medical emergencies. During lifetime, thyroid disor...
A new series of neutral, thiocyanate-free Ru(II) sensitizers (TFRS-1-3), which are assembled using both 4,4'-carboxy-2,2'-bypyridine and 2-pyridyl pyrazolate ancillaries, exhibit a light-harvesting capability up to 700 nm and superior DSSC performance in conversion efficiency (eta = 9.54% for TFRS-2).
Nucleophilic cycloaddition of thiocyanates 1a-e with C60 in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene afforded C60-fused 2-iminotetrahydrothiophene derivatives 2a-e and methanofullerenes 3a-d. The product distributions were highly sensitive to the substrates employed. The 2-iminotetrahydrothiophene derivatives 2a-e could be further manipulated by hydrolysis and acetylation to give 2-ox...
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