Simone Donato*, , , Rachele Bini, , , Giovanni Simonetti, , , Neri Fuochi, , , Martina Salzano de Luna, , , Camille Chatard, , , Pierre-Louis Brient, , , Diederik S. Wiersma, , , Daniele Martella*, , and , Camilla Parmeggiani,
{"title":"What Is the Right Chain Length? Liquid Crystalline Network Tuning by Molecular Design","authors":"Simone Donato*, , , Rachele Bini, , , Giovanni Simonetti, , , Neri Fuochi, , , Martina Salzano de Luna, , , Camille Chatard, , , Pierre-Louis Brient, , , Diederik S. Wiersma, , , Daniele Martella*, , and , Camilla Parmeggiani, ","doi":"10.1021/acs.macromol.5c01011","DOIUrl":null,"url":null,"abstract":"<p >Liquid crystalline networks (LCNs) are stimuli-responsive polymers with programmable actuation properties, including fast response times and tunable force generation. Their reversible deformations can be achieved under light irradiation when polymers are functionalized with photoresponsive molecules such as azobenzenes. All of these features need to be adapted for each specific application, and this is possible by tuning the material properties through molecular design. In this study, we demonstrate how to tailor both mechanical properties and light-dependent force development thanks to the synthesis of mesogenic cross-linkers with different alkyl chains. Acting on this molecular parameter allows modulating the maximum actuation force, while modifying the cross-linking degree is a more advantageous strategy to get fast activation. Our results provide valuable insights into the relationship between the molecular structure and material performance, paving the way for a rational design of innovative responsive materials.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 18","pages":"9672–9681"},"PeriodicalIF":5.2000,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.macromol.5c01011","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.5c01011","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Liquid crystalline networks (LCNs) are stimuli-responsive polymers with programmable actuation properties, including fast response times and tunable force generation. Their reversible deformations can be achieved under light irradiation when polymers are functionalized with photoresponsive molecules such as azobenzenes. All of these features need to be adapted for each specific application, and this is possible by tuning the material properties through molecular design. In this study, we demonstrate how to tailor both mechanical properties and light-dependent force development thanks to the synthesis of mesogenic cross-linkers with different alkyl chains. Acting on this molecular parameter allows modulating the maximum actuation force, while modifying the cross-linking degree is a more advantageous strategy to get fast activation. Our results provide valuable insights into the relationship between the molecular structure and material performance, paving the way for a rational design of innovative responsive materials.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.