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Name: supporting (supporting) for article Date: 2015-09-18 00:00:00 UTC Description: Synthetic and characterizing data for all new compounds(PDF)Crystallographic data for all X-ray ... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/jacs.5b08614/suppl_file/ja5b08614_si_002.cif Article: Facile Reversibility by Design: Tuning Small Molecule Capture and Activation by Single Component Frustrated Lewis Pairs
Name: supporting (supporting) for article Date: 2016-03-04 00:00:00 UTC Description: Experimental details and data (PDF)Crystallographic data (CIF)■ AUTHOR INFORMATION DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/jacs.6b01170/suppl_file/ja6b01170_si_002.cif Article: Catalytic B–N Dehydrogenation Using Frustrated Lewis Pairs: Evidence for a Chain-Growth Coupling Mechanism
Name: om501252m_si_002.cif Date: 2015-02-09 00:00:00 UTC Description: Supplementary data for Reactivity of Boryl- and Silyl-Substituted Carbenoids toward Alkynes: Ins... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/om501252m/suppl_file/om501252m_si_002.cif?cookieSet=1 Article: Reactivity of Boryl- and Silyl-Substituted Carbenoids toward Alkynes: Insertion and Cycloaddition Chemistry
Name: om5008055_si_002.cif Date: 2015-04-30 00:00:00 UTC Description: Supplementary data for Chiral Wide-Bite-Angle Diphosphine Ligands: Synthesis, Coordination Chemi... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/om5008055/suppl_file/om5008055_si_002.cif?cookieSet=1 Article: Chiral Wide-Bite-Angle Diphosphine Ligands: Synthesis, Coordination Chemistry, and Application in Pd-Catalyzed Allylic Alkylation
Name: ja6b00710_si_002.cif Date: 2016-03-28 00:00:00 UTC Description: Supplementary data for Enabling and Probing Oxidative Addition and Reductive Elimination at a Gr... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/jacs.6b00710/suppl_file/ja6b00710_si_002.cif?cookieSet=1 Article: Enabling and Probing Oxidative Addition and Reductive Elimination at a Group 14 Metal Center: Cleavage and Functionalization of E–H Bonds by a Bis(boryl)stannylene
Name: ja5b09913_si_002.cif Date: 2015-11-30 00:00:00 UTC Description: Supplementary data for Greater than the Sum of Its Parts: A Heterodinuclear Polymerization Catalyst DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/jacs.5b09913/suppl_file/ja5b09913_si_002.cif?cookieSet=1 Article: Greater than the Sum of Its Parts: A Heterodinuclear Polymerization Catalyst
Name: ja5062467_si_009.cif Date: 2014-07-28 00:00:00 UTC Description: Supplementary data for Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal ... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/ja5062467/suppl_file/ja5062467_si_009.cif?cookieSet=1 Article: Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal Centers: Reactivity of Five-Valence-Electron MX2 Radicals
Name: ja5062467_si_008.cif Date: 2014-07-28 00:00:00 UTC Description: Supplementary data for Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal ... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/ja5062467/suppl_file/ja5062467_si_008.cif?cookieSet=1 Article: Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal Centers: Reactivity of Five-Valence-Electron MX2 Radicals
Name: ja5062467_si_007.cif Date: 2014-07-28 00:00:00 UTC Description: Supplementary data for Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal ... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/ja5062467/suppl_file/ja5062467_si_007.cif?cookieSet=1 Article: Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal Centers: Reactivity of Five-Valence-Electron MX2 Radicals
Name: ja5062467_si_006.cif Date: 2014-07-28 00:00:00 UTC Description: Supplementary data for Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal ... DOI: Location: https://pubs.acs.org/doi/suppl/10.1021/ja5062467/suppl_file/ja5062467_si_006.cif?cookieSet=1 Article: Oxidative Bond Formation and Reductive Bond Cleavage at Main Group Metal Centers: Reactivity of Five-Valence-Electron MX2 Radicals