Sulfur isotope fractionation during incorporation of sulfur nucleophiles into organic compounds

Alon Amrani; Qisheng Ma; Ward Said Ahmad; Zeev Aizenshtat; Yongchun Tang

doi:10.1039/b717113g

Sulfur isotope fractionation during incorporation of sulfur nucleophiles into organic compounds

Alon Amrani^*, Qisheng Ma, Ward Said Ahmad, Zeev Aizenshtat, Yongchun Tang

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

26 Scopus citations

Abstract

³⁴S enrichment is shown to occur during sulfurization reactions and for the first time conclusively attributed to an isotope equilibrium effect rather than selective addition of ³⁴S enriched nucleophiles.

Original language	English
Pages (from-to)	1356-1358
Number of pages	3
Journal	Chemical Communications
Issue number	11
DOIs	https://doi.org/10.1039/b717113g
State	Published - 2008
Externally published	Yes

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title = "Sulfur isotope fractionation during incorporation of sulfur nucleophiles into organic compounds",

abstract = "34S enrichment is shown to occur during sulfurization reactions and for the first time conclusively attributed to an isotope equilibrium effect rather than selective addition of 34S enriched nucleophiles.",

author = "Alon Amrani and Qisheng Ma and Ahmad, \{Ward Said\} and Zeev Aizenshtat and Yongchun Tang",

year = "2008",

doi = "10.1039/b717113g",

language = "אנגלית",

pages = "1356--1358",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "11",

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TY - JOUR

T1 - Sulfur isotope fractionation during incorporation of sulfur nucleophiles into organic compounds

AU - Amrani, Alon

AU - Ma, Qisheng

AU - Ahmad, Ward Said

AU - Aizenshtat, Zeev

AU - Tang, Yongchun

PY - 2008

Y1 - 2008

N2 - 34S enrichment is shown to occur during sulfurization reactions and for the first time conclusively attributed to an isotope equilibrium effect rather than selective addition of 34S enriched nucleophiles.

AB - 34S enrichment is shown to occur during sulfurization reactions and for the first time conclusively attributed to an isotope equilibrium effect rather than selective addition of 34S enriched nucleophiles.

UR - https://www.scopus.com/pages/publications/41749110496

U2 - 10.1039/b717113g

DO - 10.1039/b717113g

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

C2 - 18389132

AN - SCOPUS:41749110496

SN - 1359-7345

SP - 1356

EP - 1358

JO - Chemical Communications

JF - Chemical Communications

IS - 11

ER -

Sulfur isotope fractionation during incorporation of sulfur nucleophiles into organic compounds

Abstract

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