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step decrease » sizes decrease (Expand Search), teer decrease (Expand Search)
we decrease » _ decrease (Expand Search), nn decrease (Expand Search), teer decrease (Expand Search)
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1961
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1962
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1963
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1964
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1965
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1966
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1967
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1968
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1969
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1970
Optical Effects of <i>S</i>-Oxidation and M<sup><i>n</i>+</sup> Binding in <i>meso</i>-Thienyl Dipyrrin Systems and of Stepwise Bromination of 4,4-Difluoro-8-(2,5-dibromo-3-thienyl...
Published 2008“…<i>meso</i>-Thienyl group properties were revealed through the use of 3,4,4-triphenyl-8-(thienyl)-4-bora-3<i>a</i>,4<i>a</i>-diaza-<i>s</i>-indacene; Cu<sup>2+</sup> addition resulted in smooth absorption decreases which were modeled to support 1:1 substrate:M<sup>2+</sup> binding; for Hg<sup>2+</sup> 1:2 substrate:M<sup>2+</sup> binding was found. …”
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1971
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1972
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1973
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1974
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1975
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1976
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1977
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1978
Ligand-Controlled Magnetic Interactions in Mn<sub>4</sub> Clusters
Published 2009“…Experimentally measured magnetic moments in high magnetic fields show that, upon electron density withdrawal, the main antiferromagnetic exchange constant <i>J</i><sub>1</sub> decreases from −2.2 K for the [Mn<sub>4</sub>(OAc)<sub>4</sub>] cluster to −1.9 K for the [Mn<sub>4</sub>(H<sub>5</sub>C<sub>6</sub>COO)<sub>4</sub>] cluster and −0.6 K for the [Mn<sub>4</sub>(F<sub>3</sub>CCOO)<sub>4</sub>] cluster, while <i>J</i><sub>2</sub> decreases from −1.1 K to nearly 0 K and <i>J</i><sub>3</sub> changes to a small ferromagnetic coupling. …”
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1979
Ligand-Controlled Magnetic Interactions in Mn<sub>4</sub> Clusters
Published 2009“…Experimentally measured magnetic moments in high magnetic fields show that, upon electron density withdrawal, the main antiferromagnetic exchange constant <i>J</i><sub>1</sub> decreases from −2.2 K for the [Mn<sub>4</sub>(OAc)<sub>4</sub>] cluster to −1.9 K for the [Mn<sub>4</sub>(H<sub>5</sub>C<sub>6</sub>COO)<sub>4</sub>] cluster and −0.6 K for the [Mn<sub>4</sub>(F<sub>3</sub>CCOO)<sub>4</sub>] cluster, while <i>J</i><sub>2</sub> decreases from −1.1 K to nearly 0 K and <i>J</i><sub>3</sub> changes to a small ferromagnetic coupling. …”
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1980
DataSheet_1_Domesticating Vigna stipulacea: Chromosome-Level genome assembly reveals VsPSAT1 as a candidate gene decreasing hard-seededness.pdf
Published 2023“…Given that there are multiple stress-tolerant wild legume species, it is important to establish efficient domestication processes using reverse genetics and identify the genes responsible for domestication traits. In this study, we identified VsPSAT1 as the candidate gene responsible for decreased hard-seededness, using a Vigna stipulacea isi2 mutant that takes up water from the lens groove. …”