将三(1-氧代-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷-4-亚甲基)磷酸酯(trimer)用于阻燃聚碳酸酯(PC),研究了它对 PC 阻燃性能、机械性能、热分解行为及灼烧残炭的影响。将 trimer 用于 PC 时,其质量分数为8%的用量即可使 PC 的阻燃级别达...将三(1-氧代-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷-4-亚甲基)磷酸酯(trimer)用于阻燃聚碳酸酯(PC),研究了它对 PC 阻燃性能、机械性能、热分解行为及灼烧残炭的影响。将 trimer 用于 PC 时,其质量分数为8%的用量即可使 PC 的阻燃级别达到 UL 94 V-O(试样厚度为3.2 mm)级,极限氧指数达33%。值得注意的是,加入 trimer 可改善 PC 的拉伸强度,特别是弯曲强度及弯曲模量。热分析数据表明,trimer 可提前并加速 PC 的交联成炭,但不能提高PC 的成炭率。此外,扫描电子最微镜照片显示,trimer 可使炭层轻微发泡膨胀,也可改善炭层质量。展开更多
Sable organic radicals are promising materials for information storage,molecular magnetism,electronic devices,and biological probes.Many organic radicals have been prepared,but most are non-or weakly emissive and degr...Sable organic radicals are promising materials for information storage,molecular magnetism,electronic devices,and biological probes.Many organic radicals have been prepared,but most are non-or weakly emissive and degrade easily upon photoexcitation.It remains challenging to produce stable and efficient luminescent radicals because of the absence of general guidelines for their synthesis.Herein,we present a photoactivation approach to generate a stable luminescent radical from tris(4-chlorophenyl)phosph ine(TCPP)with red emission in the crystal state.The mechanistic study suggests that the molecular symmetry breaking in the crystal causes changes of molecular conformation,redox properties,andmolecular packing that facilitates radical generation and stabilization.This design strategy demonstrates a straightforward approach to develop stable organic luminescent radicals that will open new doors to photoinduced luminescent radical materials.展开更多
文摘将三(1-氧代-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷-4-亚甲基)磷酸酯(trimer)用于阻燃聚碳酸酯(PC),研究了它对 PC 阻燃性能、机械性能、热分解行为及灼烧残炭的影响。将 trimer 用于 PC 时,其质量分数为8%的用量即可使 PC 的阻燃级别达到 UL 94 V-O(试样厚度为3.2 mm)级,极限氧指数达33%。值得注意的是,加入 trimer 可改善 PC 的拉伸强度,特别是弯曲强度及弯曲模量。热分析数据表明,trimer 可提前并加速 PC 的交联成炭,但不能提高PC 的成炭率。此外,扫描电子最微镜照片显示,trimer 可使炭层轻微发泡膨胀,也可改善炭层质量。
基金financially supported by theNationalNatural Science Foundation of China(grant no.21788102)the NaturalScienceFoundationofGuangdongProvince(grant nos.2019B121205002 and 2019B030301003)+3 种基金the Research Grants Council of Hong Kong(grant nos.16305618,16305518,C6014-20W,C6009-17G,and AoE/P-02/12)the National Key Research and Development Program(grant no.2018YFE0190200)the Innovation and Technology Commission(grant no.ITC-CNERC14SC01)the Science and Technology Plan of Shenzhen(grant nos.JCYJ20180306174910791,JCYJ20170818113530705,JCY J20170818113538482,and JCYJ20160229205601482).
文摘Sable organic radicals are promising materials for information storage,molecular magnetism,electronic devices,and biological probes.Many organic radicals have been prepared,but most are non-or weakly emissive and degrade easily upon photoexcitation.It remains challenging to produce stable and efficient luminescent radicals because of the absence of general guidelines for their synthesis.Herein,we present a photoactivation approach to generate a stable luminescent radical from tris(4-chlorophenyl)phosph ine(TCPP)with red emission in the crystal state.The mechanistic study suggests that the molecular symmetry breaking in the crystal causes changes of molecular conformation,redox properties,andmolecular packing that facilitates radical generation and stabilization.This design strategy demonstrates a straightforward approach to develop stable organic luminescent radicals that will open new doors to photoinduced luminescent radical materials.
