Summary

使用苝作为可见光光催化功能化的乙烯基单体原子转移自由基聚合

Published: April 22, 2016
doi:

Summary

A method for the atom transfer radical polymerization of functionalized vinyl monomers using perylene as a visible-light photocatalyst is described.

Abstract

A standardized technique for atom transfer radical polymerization of vinyl monomers using perylene as a visible-light photocatalyst is presented. The procedure is performed under an inert atmosphere using air- and water-exclusion techniques. The outcome of the polymerization is affected by the ratios of monomer, initiator, and catalyst used as well as the reaction concentration, solvent, and nature of the light source. Temporal control over the polymerization can be exercised by turning the visible light source off and on. Low dispersities of the resultant polymers as well as the ability to chain-extend to form block copolymers suggest control over the polymerization, while chain end-group analysis provides evidence supporting an atom-transfer radical polymerization mechanism.

Introduction

The synthesis of technologically advanced polymers requires precise control over polymer molecular weight, dispersity (Ð), composition, and architecture.1,2 Controlled radical polymerizations (CRPs)3-8 have revolutionized the synthesis of well-defined polymers, with atom transfer radical polymerization (ATRP) being the most used CRP, largely due to operational simplicity and synthetic versatility.9-14 The crux of ATRP is the ability to reversibly deactivate the polymerization, controlling the equilibrium between a propagating radical and a dormant species. Enforcing a low concentration of active radicals greatly minimizes bimolecular termination pathways and allows for the synthesis of well-defined polymers.

Traditional ATRP relies on a transition metal catalyst to mediate this equilibrium.3 These metal catalysts contaminate the polymer product and impede implementation in biomedical or electronic applications while also raising environmental concerns. Although significant strides have been made to reduce the catalyst concentration to ppm levels, these methodologies require more demanding experimental conditions and metal contamination is still not entirely eliminated.15,16

Reversible addition-fragmentation transfer17,18 and nitroxide-mediated polymerizations19,20 are CRPs that do not require metal catalysts, although they have been used less often than ATRP.3 Recently, reversible chain-transfer21 and reversible complexation22,23 variants of ATRP that can use organic catalysts were reported. However, these methodologies require the use of alkyl iodide initiators and are not effective with the alkyl bromides commonly employed in ATRP. A highly desirable CRP would match the performance, feasibility, and robustness of traditional ATRP while being catalyzed by an organic catalyst under mild conditions.

Here, we describe a methodology for the radical polymerization of functionalized vinyl monomers using perylene as a visible-light photocatalyst. Through optimization of parameters such as stoichiometry, concentration, time, and light flux, the molecular weight of the polymers can be controlled.24, 25 Similar methodologies have been recently introduced using phenothiazine derivatives as photocatalysts for metal-free ATRP.26, 27 Because researchers in the field of polymerization catalysis are constantly developing new catalytic systems, the ability to compare catalyst performance across a number of metrics is vital. This ability to make comparisons relies heavily upon procedural consistency and clarity on the part of the researchers performing the experiments. As such, it is our goal that this video will be used to help precisely communicate the methods by which these polymers are synthesized and characterized.

Protocol

小心:许多在此协议中使用的化学品是有害物质。查阅材料安全数据表(MSDS),并与这些物质时使用适当的个人防护装备(PPE)。 1.净化,准备和试剂的存储提纯,使用根据制造商的协议的溶剂纯化系统中使用的所有溶剂。如果溶剂净化系统不可用时,使用干燥剂( 例如,分子筛,氢化钙2 等 )和蒸馏。一旦干燥,储存溶剂在氮气氛下在室温下…

Representative Results

表1示出了聚合结果通过该方法达到的范围内。这些数据表明,苝能够用作许多官能化的乙烯基单体的聚合的光催化剂。对于一个特定的单体中的任一数目的反应参数,如溶剂,化学计量,引发剂,和光源的调整导致聚合物具有不同的分子量和分散度从非常好到相当宽的。 图1示出了链-的结果延伸实验如在第4部分描述的,并表明使用该方法形成的…

Discussion

虽然该协议演示此聚合技术的一个具体的例子,提供给研究者进行该反应的选择相当广阔。修饰可以在若干点进行整个协议,以允许任何特定photoredox的正在执行的ATRP的优化。随着新的单体,引发剂,以及用于该反应在调查来催化剂中,化学计量学和溶剂用于执行能够反应并且应修改的反应条件的优化的一部分。此外,从个人实验者可以选择使用表1作为一个准则来修改其他参数,如?…

Divulgations

The authors have nothing to disclose.

Acknowledgements

The authors would like to acknowledge the University of Colorado Boulder for its support of this work.

Materials

perylene, min 98.0% TCI America TCP0078-025G purify by sublimation
N,N-dimethylformamide VWR EM-DX1726-1 Omnisolv
methyl methacrylate, 99% VWR 200000-678 distilled prior to use, stored in refrigerator
ethyl α-bromophenyl acetate  Aldrich 554065 distilled prior to use stored in refrigerator
butylated hydroxytoluene  Aldrich W218405
Chloroform-D Cambridge Isotope Labs DLM-7-100
tetrahydrofuran VWR EM-TX0279-1 Omnisolv
methanol VWR BDH1135
dichloromethane VWR EM-DX0831-1 Omnisolv
styrene, 99% VWR AAAA18481-0F distilled prior to use, stored in refrigerator
glass scintillation vial, 20 mL VWR 66022-065
screw top vial, 2 mL Agilent 5182-0715
septum cap for screw top vial Agilent 5182-0717
heavy wall pressure vessel, 100 mL Synthware P160005 
syringe, 1 mL norm-ject VWR 89174-491
NMR tube New Era NE-UL5-7'
nylon syringe filter, 0.45 um VWR 28143-240
glovebox Mbraun LABstar
solvent purification system Mbraun MB-SPS-800
stirplate IKA 3582401
light-emitting diodes Creative Lighting Solutions CL-FRS1210-5M-12V-WH 2x 12-inch strips of 5500 K white LEDs were used for illumination
12V DC power supply for LEDs Creative Lighting Solutions CL-PS16001-40W
high performance liquid chromatograph  Agilent G1310B, G1322A, G1329B, G1316A
gel permeation size-exclusion columns Agilent PL1110-6500
multi-angle light scattering detector Wyatt WTREOS
differential refractometer Wyatt WTREX

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Theriot, J. C., Ryan, M. D., French, T. A., Pearson, R. M., Miyake, G. M. Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst. J. Vis. Exp. (110), e53571, doi:10.3791/53571 (2016).

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