Search alternatives:
we decrease » _ decrease (Expand Search), teer decrease (Expand Search), use decreased (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
1 we » _ we (Expand Search), 1 w (Expand Search), 1 wt (Expand Search)
we decrease » _ decrease (Expand Search), teer decrease (Expand Search), use decreased (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
1 we » _ we (Expand Search), 1 w (Expand Search), 1 wt (Expand Search)
-
1801
-
1802
-
1803
-
1804
-
1805
-
1806
-
1807
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. …”
-
1808
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. …”
-
1809
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. …”
-
1810
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. …”
-
1811
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. …”
-
1812
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. …”
-
1813
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. …”
-
1814
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. …”
-
1815
-
1816
-
1817
-
1818
-
1819
-
1820