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Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

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Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
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Structure and Nomenclature of Thiols and Sulfides02:17

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Thiols and sulfides are sulfur analogs of alcohols and ethers, respectively, where the sulfur atom takes the place of the oxygen atom. Thus, thiols are generally represented as RSH, where R is an alkyl substituent and —SH is the functional group. On the other hand, in sulfides, the central sulfur atom is bonded to two hydrocarbon groups on either side. Depending upon the type of group, sulfides can be either symmetrical or asymmetrical. Both thiols and sulfides display a bent geometry,...
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Preparation and Reactions of Thiols02:33

Preparation and Reactions of Thiols

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Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
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Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
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Hydrogen Bonds

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A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
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Hydrogen sulfide in stroke: Protective or deleterious?

Su Jing Chan1, Peter T-H Wong2

  • 1Institute of Medical Biology, Agency for Science, Technology and Research (A*STAR), Singapore; Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, USA.

Neurochemistry International
|February 9, 2017
PubMed
Summary

Hydrogen sulfide (H₂S) acts as a signaling molecule in the central nervous system. Its role in stroke is concentration-dependent, potentially offering protection at low levels and causing harm at high levels.

Keywords:
Hydrogen sulphideNeuroprotectionStrokeToxic effect

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Area of Science:

  • Neuroscience
  • Biochemistry
  • Pathology

Background:

  • Hydrogen sulfide (H₂S) is recognized as a signaling molecule in the central nervous system.
  • H₂S levels increase rapidly in the brain following ischemic insults, such as in experimental stroke models.

Purpose of the Study:

  • To review and synthesize current literature on the role of hydrogen sulfide in ischemic stroke.
  • To determine whether H₂S is protective or deleterious in the context of stroke.

Main Methods:

  • Literature review of studies investigating hydrogen sulfide in experimental stroke.
  • Analysis of evidence regarding the effects of H₂S concentration on ischemic brain injury.

Main Results:

  • Current evidence does not provide a definitive answer regarding the role of H₂S in stroke.
  • The effect of H₂S appears to be concentration-dependent: high concentrations may be deleterious, while low concentrations may be protective.

Conclusions:

  • The dual role of H₂S in ischemic stroke suggests a complex involvement.
  • Modulating H₂S concentration (either increasing or decreasing it) may represent a potential therapeutic strategy for stroke treatment.