Synthesis of Single-Crystal Two-Dimensional Covalent Organic Frameworks and Uncovering Their Hidden Structural Features by Three-Dimensional Electron Diffraction

化学 共价键 电子衍射 单晶 衍射 结晶学 电子 化学物理 纳米技术 有机化学 光学 量子力学 物理 材料科学
作者
Lejian Deng,Wantao Chen,Guojun Zhou,Ying Liu,Lingmei Liu,Yu Han,Zhehao Huang,Donglin Jiang
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
被引量:14
标识
DOI:10.1021/jacs.4c14535
摘要

Two-dimensional covalent organic frameworks (2D COFs) are formed by the polycondensation of geometrically specific monomers to grow covalently connected 2D polygonal polymers over the a–b plane and supramolecular polymerization and/or crystallization of 2D sheets along the c direction to constitute layer architectures. Despite various efforts, the synthesis of single-crystal 2D COFs remains a challenging goal. Here, we report the synthesis of single-crystal 2D COFs, by taking the representative imine-linked TPB-DMTP-COF as an example, to reveal the key synthetic parameters that control the crystallization of 2D COFs. We systematically tune the synthetic conditions including the glassware setup, the degas method, the solvent, the temperature, the modulator, and the reaction time and observed that all these parameters greatly affect the polymerization and crystallization processes, controlling the crystal quality. We found that a homogeneous system with all components dissolved and the presence of a suitable modulator at a temperature of 50–70 °C allows the growth of TPB-DMTP-COF single crystals as isolated individual rods, with tunable diameters of 200 nm to 3 μm and a length of 1–20 μm. The single-crystal structure was characterized by three-dimensional electron diffraction (3DED), which revealed two conformations of trans and cis for the linker in the 2D polymer sheets, which stack in an antiparallel mode to shape the frameworks with double-sized unit cells. These results uncover these hidden structural features which have been overlooked in polycrystalline and single-crystal studies and provide new insights into the synthesis of high-quality single crystals of 2D COFs.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
Aria发布了新的文献求助10
刚刚
科研通AI5应助缥缈的铅笔采纳,获得10
刚刚
詹子阳完成签到,获得积分20
1秒前
我是老大应助cyq采纳,获得10
1秒前
量子星尘发布了新的文献求助10
1秒前
芝芝完成签到,获得积分10
2秒前
maodou发布了新的文献求助10
2秒前
3秒前
詹子阳发布了新的文献求助10
3秒前
公孙玲珑完成签到,获得积分10
4秒前
5秒前
大力半鬼完成签到,获得积分10
5秒前
FashionBoy应助王荣超采纳,获得10
6秒前
BING发布了新的文献求助10
7秒前
LJD发布了新的文献求助10
8秒前
李升洋完成签到 ,获得积分10
8秒前
8秒前
科研通AI6应助2224536采纳,获得10
9秒前
早期早睡完成签到,获得积分10
9秒前
香蕉觅云应助maodou采纳,获得10
9秒前
Orange应助zz采纳,获得10
10秒前
10秒前
科研通AI6应助小芦铃采纳,获得10
11秒前
www发布了新的文献求助10
11秒前
11秒前
金戈完成签到,获得积分10
12秒前
翼德救我i应助橘子采纳,获得10
12秒前
英俊的铭应助nusaber采纳,获得10
13秒前
量子星尘发布了新的文献求助10
13秒前
tpl发布了新的文献求助10
13秒前
13秒前
科研通AI5应助achulw采纳,获得10
14秒前
科研通AI2S应助windows采纳,获得10
14秒前
甜蜜的面包关注了科研通微信公众号
15秒前
15秒前
月月发布了新的文献求助10
15秒前
www完成签到,获得积分10
16秒前
英姑应助wxy采纳,获得10
16秒前
雷家发布了新的文献求助10
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Zeolites: From Fundamentals to Emerging Applications 1500
Encyclopedia of Materials: Plastics and Polymers 1000
Architectural Corrosion and Critical Infrastructure 1000
Early Devonian echinoderms from Victoria (Rhombifera, Blastoidea and Ophiocistioidea) 1000
Hidden Generalizations Phonological Opacity in Optimality Theory 1000
Handbook of Social and Emotional Learning, Second Edition 900
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 4920881
求助须知:如何正确求助?哪些是违规求助? 4192265
关于积分的说明 13020962
捐赠科研通 3963415
什么是DOI,文献DOI怎么找? 2172449
邀请新用户注册赠送积分活动 1190294
关于科研通互助平台的介绍 1099258