The mechanism of ring‐opening polymerization of L‐lactide by ICl3 catalysts: Halogen bond catalysis or participating in reactions?

The mechanism of ring‐opening polymerization of L‐lactide by iodine trichloride (ICl3) catalyst has been explored by using density functional theory (DFT) calculations and three catalytic pathways were proposed. The first and second pathways belong to the halogen bond catalysis, and the third pathway involves the ICl3 catalysts participating in reactions. When the carbonyl group was maintained involved in the reaction and activated catalytically by the halogen bond, there are two possible pathways. The first pathway involves only one transition state, and the second pathway requires two transition states. There is another pathway in which ICl3 directly participates in the reaction, it is named the third pathway. Two different transition states of the four‐membered rings are generated successively, the transfer of I─O bonds determined the progress of the reaction. Theoretical calculations in this work provide the most basic understanding of ring‐opening polymerization of L‐lactide by ICl3 catalysts. © 2019 Wiley Periodicals, Inc.

[1]  Clark R. Landis,et al.  NBO 6.0: Natural bond orbital analysis program , 2013, J. Comput. Chem..

[2]  Michael Dolg,et al.  A theoretical study of imine hydrocyanation catalyzed by halogen‐bonding , 2015, J. Comput. Chem..

[3]  Cheng Chang,et al.  Properties of atoms in molecules: atomic volumes , 1987 .

[4]  Timothy Clark,et al.  Halogen bonding: the σ-hole , 2007 .

[5]  P. Kongsaeree,et al.  Bis(pyrrolidene) Schiff Base Aluminum Complexes as Isoselective-Biased Initiators for the Controlled Ring-Opening Polymerization of rac-Lactide: Experimental and Theoretical Studies , 2015 .

[6]  H. Stoll,et al.  Systematically convergent basis sets with relativistic pseudopotentials. II. Small-core pseudopotentials and correlation consistent basis sets for the post-d group 16–18 elements , 2003 .

[7]  K. Morokuma,et al.  Mechanism of Metal-Free C-H Activation of Branched Aldehydes and Acylation of Alkenes Using Hypervalent Iodine Compound: A Theoretical Study. , 2015, The Journal of organic chemistry.

[8]  Thom H. Dunning,et al.  Gaussian basis sets for use in correlated molecular calculations. V. Core-valence basis sets for boron through neon , 1995 .

[9]  M. Reiher,et al.  Engineering Molecular Iodine Catalysis for Alkyl–Nitrogen Bond Formation , 2018 .

[10]  Peter Politzer,et al.  Quantitative analysis of molecular surfaces: areas, volumes, electrostatic potentials and average local ionization energies , 2010, Journal of molecular modeling.

[11]  Min Zhu,et al.  Assessment of intermolecular interactions at three sites of the arylalkyne in phenylacetylene‐containing lithium‐bonded complexes: Ab initio and QTAIM studies , 2012, J. Comput. Chem..

[12]  Yanli Zeng,et al.  Improvement in dehydrogenation performance of Mg(BH4)2·2NH3 doped with transition metal: First-principles investigation , 2015 .

[13]  P. Dubois,et al.  Controlled room temperature ROP of L-lactide by ICl3: a simple halogen-bonding catalyst , 2010 .

[14]  C. Cramer,et al.  Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions. , 2009, The journal of physical chemistry. B.

[15]  R. Kuchta,et al.  Activation of Michael Acceptors by Halogen-Bond Donors , 2017, Synlett.

[16]  S. Papson “Model” , 1981 .

[17]  Jie Lv,et al.  Preparation of Curcumin-Piperazine Coamorphous Phase and Fluorescence Spectroscopic and Density Functional Theory Simulation Studies on the Interaction with Bovine Serum Albumin. , 2017, Molecular pharmaceutics.

[18]  H. Hibbert USE OF IODINE AS A DEHYDRATING AND CONDENSING AGENT. , 1915 .

[19]  Guan-Wen Yang,et al.  Highly Robust Yttrium Bis(phenolate) Ether Catalysts for Excellent Isoselective Ring-Opening Polymerization of Racemic Lactide , 2017 .

[20]  L. Maron,et al.  Theoretical Investigation of Lactide Ring-Opening Polymerization Induced by a Dinuclear Indium Catalyst , 2013 .

[21]  Burke,et al.  Generalized Gradient Approximation Made Simple. , 1996, Physical review letters.

[22]  J. Murray,et al.  The σ-hole revisited. , 2017, Physical chemistry chemical physics : PCCP.

[23]  T. H. Dunning Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen , 1989 .

[24]  Akira Yoshimura,et al.  Advances in Synthetic Applications of Hypervalent Iodine Compounds. , 2016, Chemical reviews.

[25]  T. Dunning,et al.  Electron affinities of the first‐row atoms revisited. Systematic basis sets and wave functions , 1992 .

[26]  Lingpeng Meng,et al.  The competition of Y⋯o and X⋯n halogen bonds to enhance the group V σ‐hole interaction in the NCY⋯oPH3⋯NCX and OPH3⋯NCX⋯NCY (X, YF, Cl, and Br) complexes , 2015, J. Comput. Chem..

[27]  J. Murray,et al.  Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts , 2017, IUCrJ.

[28]  S. Huber,et al.  Activation of a carbonyl compound by halogen bonding. , 2014, Chemical communications.

[29]  K. Noguchi,et al.  Molecular-Iodine-Catalyzed Cyclization of 2-Alkynylanilines via Iodocyclization-Protodeiodination Sequence. , 2017, Organic letters.