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There were in all 702 hits containing 1,2-diphenylactylene. In most of them (676), the acetylenic bond had undergone pi-allyl complexation and hence these structures have not been used in this study.
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There were in all 702 hits containing 1,2-diphenylactylene. In most of them (676), the acetylenic bond had undergone pi-allyl complexation and hence these structures have not been used in this study.
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Of the 26 hits, two are duplicates and three do not contain 3D coordinates. Besides these, we have been able to crystallize 1,2-diphenylacetylene in an orthorhombic lattice containing single planar molecule which we have reported recently cede ref. No: 606397, However, as the crystal was unstable, it could not be used for charge density data collection. Including the polymorph presented in this paper, the total number of structures used in our analysis will be 23
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Of the 26 hits, two are duplicates and three do not contain 3D coordinates. Besides these, we have been able to crystallize 1,2-diphenylacetylene in an orthorhombic lattice containing single planar molecule which we have reported recently (cede ref. No: 606397). However, as the crystal was unstable, it could not be used for charge density data collection. Including the polymorph presented in this paper, the total number of structures used in our analysis will be 23.
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41
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84906359310
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2 values. Such large distortions in their molecular structure with unusual bond lengths are due to solid-state effects, namely, OH-π interactions as in GAWLEV, π-π interactions as in JOXLIR, and regio constraints due to steric class of repulsions as in BETDEJ and EBAWUA. (See Supplementary Table for the refcodes.)
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2 values. Such large distortions in their molecular structure with unusual bond lengths are due to solid-state effects, namely, OH-π interactions as in GAWLEV, π-π interactions as in JOXLIR, and regio constraints due to steric class of repulsions as in BETDEJ and EBAWUA. (See Supplementary Table for the refcodes.)
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