dc.contributor.author |
Nagarajan, K. |
|
dc.contributor.author |
Chaudhury, P.K. |
|
dc.contributor.author |
Srinivasan, B.R. |
|
dc.contributor.author |
Sarkar, S. |
|
dc.date.accessioned |
2015-06-03T07:29:22Z |
|
dc.date.available |
2015-06-03T07:29:22Z |
|
dc.date.issued |
2001 |
|
dc.identifier.citation |
Chemical Communications. (18); 2001; 1786-1787. |
en_US |
dc.identifier.uri |
http://dx.doi.org/10.1039/b105341h |
|
dc.identifier.uri |
http://irgu.unigoa.ac.in/drs/handle/unigoa/1244 |
|
dc.description.abstract |
pH dependent reactivity differences of dimethylsulfite towards the title complex 1 demonstrate the crucial need of oxo-anionic coordination of sulfite to the molybdenum centre of 1 in the model reductive half reaction of sulfite oxidase. |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Chemistry |
en_US |
dc.title |
Oxoanionic or sulfur lone pair attack? The difference in reactivity of hydrogensulfite anion and neutral dimethylsulfite towards [Bu4N](2)[MoO2{S2C2(CN)(2)}(2)] in the model reductive half reaction of sulfite oxidase |
en_US |
dc.type |
Journal article |
en_US |
dc.identifier.impf |
y |
|