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Special Report                                                                                                                                                                   Special Report


                                                                          synthesized by controlling the Pd load-    High-effi ciency direct            sured  activity and  chemical composi-  catalyst partially dissolves under hydro-
                                                                          ing  amount  and preparation  methods,     esterifi cation of CO  and         tion is reported. (Ind. Eng. Chem. Res.,  formylation  conditions.  Cyclohexene
                                                                                                                                         2
                                                                          on the title  conversion of practical      methanol over Co-doped CeO        2025; DOI: 10.1021/acs.iecr.5c00026).  was  used  as  an  olefi n  at  40  bar  and
                                                                          interest. The nanocluster catalyst gave    catalysts                      2                                    100°C.  Heterogeneous separation was
                                                                          relatively  high hydrogenation  activity.                                    Enhanced stability and            done. Long-chain C -C alkenes, alpha-
                                                                                                                                                                                                           18
                                                                                                                                                                                                         6
                                                                          (Chem. Commun., 2025/DOI:10.1039/          C. Xue et al have worked on the title   activity in upgrading ethanol   methylstyrene and mixed octenes were
       cent breakthrough and perspectives are  monomers  in  up  to  98%.  Blends  of  D4CC05105J).                  reaction to make dimethyl carbonate   (E) to n-butanol (B) using a   studied. (Ind. Eng. Chem. Res., 2025;
       discussed. (ChemSusChem, 2024; DOI:  polymers can also be processed.                                          (DMC; which is obtained via exchange   Ru polyphenylene catalyst    DOI: 10.1021/acs.iecr.4c03886).
       10.1002/cssc.202402335).                                           Ketonization of valeric acid to            reaction of  ethylene carbonate with
                                         Inverting methanol               5-nonanone                                 CH OH). The chemical stability of CO    X.  Pei  et  al have  compared homo- Production of xylenes from
                                                                                                                        3
                                                                                                                                                    2
       Catalyst improved                 dehydrogenation selectivity                                                 makes this reaction diffi cult. A series of   geneous and heterogeneous catalysts in  heavy reformate (HR)
       stereoselectivity and             by crowding atomic Ni species    A.A. Eslami et al have screened metal      catalysts M-CeO  (M= Fe, Cu, Co, La,   Guerbet chemistry. There is a reference
                                                                                                                                   2
       regioselectivity control to       over α-MoC catalysts             oxides  for  the  title  reaction.  Good   Zr, Ni, and Al) were constructed by a   to catalyst compatible  with molecular   HR contains pseudocumene, ethyl tolue-
       access completely alternating                                      catalysts have both lattice  energy and                                      sieves for water removal, which results   nes, mesitylene, etc. and T. Kella et al
       poly(lactic acid-co-glycolic      Y. Ge et al have referred to metal car-  amphoteric properties. ZrO  was found                                in enhanced B yields. In situ reduction   have worked on converting this C9+
                                                                                                2
                                                                                                                                                                                         cut into xylenes. This review highlights
       acid) (PLGA) with enhanced        bides as promising alternatives of noble  to be the most active catalyst. Tempera-                            of Ru polyphenylene catalyst was car-  the role of zeolite catalysts in improv-
       properties                        metal  catalysts. However, the precise  ture was in the range of 350-450°C.                                   ried out to form Ru nanocluster during   ing product selectivity and focuses on
                                                                                                                                                       Guerbet reaction. Detailed functioning
                                         control  of reaction  pathways  on them  The catalysts were fully characterised
                                         remains a formidable challenge. When  and by products were also analysed.                                     of the catalyst  is reported.  (Applied   catalyst  modifi cations  and  topologies.
       X. Guo  et al have referred to the   α-MoC  is  decorated  with  crowding  (ChemCatChem., 2024; DOI:  1002/                                     Catalysis A:  General, 2025, 694, 25   The effects of  incorporating various
       title  polymer as an ideal candidate   atomic Ni species, CH OH goes to CO  cctc.202401467).                                                    March, 120139; DOI:10.1016/j.apca-  metals in zeolites on the product selec-
                                                           3
       for controlled  drug delivery.  These   + H .  Under  optimal  conditions,  ex-                               doping strategy. 2-Cyanopyridine (CP)  ta.2025.120139).             tivity and yield are reported. Aspects of
       authors have used the chiral (BisSalen)  cellent selectivities of the target com-  Molecularly defi ned lubricant   was employed  as a  dehydrating  agent                         catalyst deactivation and  regeneration
                                            2
       Al catalyst,  which promoted a robust   pound (over 90%) can be achieved in   hydrocarbons from olefi n        to  facilitate  the  esterifi cation  reaction.   Glycerol (G) to AA  are discussed. Aspects of reactor engi-
       polymerisation of enantiopure 3-methyl   both cases  with unprecedented pro-                                  Under  optimal  conditions  61%  con-                               neering and process optimisation  are
       glycolide with  highly glycolic site   duction rates  of  methyl formate and   metathesis                     version of CH OH with 61.6% yield of  A. Kurniawan  et al have investigated  also covered. (Ind. Eng. Chem. Res.,
                                                                                                                                 3
       selectivity,  giving  alternating  PLGA   H  for different versions of the catalyst.  Z.J.  Berkson  et  al  have  referred  to   DMC was realised. Monomethyl  car-  the gas phase conversion of G to AA  2025; DOI: 10.1021/acs.iecr.4c03940).
       with regioselectivity. Degradation and   Kinetic, spectroscopic and computa-  the use of hydrocarbons based syn-  bonate was an intermediate. (Ind. Eng.  through consecutive dehydration and
                                          2
       drug  release  experiments  were  done.   tional assessments  were integrated to  thetic  lubricants.  Branched  terminal   Chem. Res., 2025; DOI: 10.1021/acs.  H  transfer reactions over Mo-V oxides  Transalkylation between
                                                                                                                                                         2
       (Angew. Chem. Intl.  Ed., 2024; DOI:   clarify the mechanism of the above re-  olefi ns were used and after metathesis   iecr.4c04628).          supported  on  acid-modifi ed  montmo- C  aromatics and
                                                                                                                                                                                           10
       10.1002/anie.202417075).          markable selectivity inversion. (Angew.  were subjected  to hydrogenation. An-                                rillonite (HMMT). The use of HMMT  2-methylnaphthalene
       Solvent-free chemical             Chem. Intl. Ed., 2024; DOI:  10.1002/  alytical  procedures were employed   In situ reduced Ni-Sn             as a support enables the well dispersion  (MN) to synthesize
                                                                                                                                                       of  metal  oxide  particles  with  nominal
       recycling of polyesters and       anie.202023682).                 to characterize the products. (Chem-       bimetallic catalyst for           loadings up to 5 wt % on the catalyst   2,6-dimethylnaphthalene
       polycarbonates by Mg-based                                         CatChem., 2024; DOI:  10.1002/cctc.        enhancing direct upgrading        surface while the acidic sites facilitate   (DMN) by Mo-modifi ed
       Lewis acid catalyst               From single atoms to             202401590).                                of aqueous ethanol to higher      dehydration of G to acrolein with 74%   HZSM-12 catalysts
                                         nanoparticles: Size effect on
                                                                                                                     alcohols
       W. Zhao et al have utilised commercially  Pd/C-catalysed hydrogenation   Carbonylation reactions using                                          selectivity. At 320°C and ambient pres-  DMN is a key raw material  to make
       available Lewis acids (LAs) to realize  of 2,5-furandicarboxylic acid  single-atom catalysts                  B. Chen et al have investigated NiSnH  sure, 22% yield of AA is reported. (Ind.   the  corresponding  dicarboxylic  acid,
       closed-loop recycling through the cata-                            L. Jurado  et al  have reviewed the re-    catalysts under various gas atmospheres  Eng. Chem. Res., 2025; DOI: 10.1021/  which in turn is used to make polyethy-
       lytic  depolymerisation  of aliphatic  J. Zheng  et  al have reported  a study   cent advances in tailoring solid sup-  and pretreatment temperatures and this  acs.iecr.4c02838).  lene  naphthalate  (PEN),  which  has
       polyesters and polycarbonates.  Thus  of fi ve catalysts with Pd particle sizes   ports for single-atom catalysts (SACs)   have infl uence on the title conversions.                some outstanding properties compared
                                                                                                                     Theoretical  insights  are reported and  A carrier-free recyclable
       poly(ε-caprolactone)  and  poly(trimethy-  ranging from single atoms to nano-  to enhance their catalytic performance                                                             to  PET.  C.  Xiong  et  al have  made  a
       lene carbonate)  were  converted to  clusters and nanoparticles, which were                                   correlative  dependence between mea-  Rh/Terpyridine catalyst for   series of Mo/HZSM-12 molecular sieve
                                                                          in the title reaction, hydroformylation,                                     alkene hydroformylation:          catalysts for the title reaction. The trans-
                                                                          methanol carbonylation, and oxidative                                        Homogeneous catalysis and         alkylation reaction was done under H
                                                                                                                                                                                                                        2
                                                                          carbonylation. Optimizing of solid sup-                                      heterogeneous separation          atmosphere.  30% Mo/HZSM-12 gave
                                                                          ports to realise highly active and selec-                                                                      excellent  performance  with  61%  con-
                                                                          tive performance is discussed. In situ/                                      H. Fang et al have synthesized a new  version  of MN and 2,6- to 2,7-DMN
                                                                          operando characterisation  of the cata-                                      square-planar geometry Rh (I) com-  ratio of 1.69. (Applied Catalysis, 2025,
                                                                          lyst is covered. (ChemCatChem., 2024;                                        plex,  Rh (CO) (Terpyridine)  and pro-  693, 5 March, 120138; DOI:10.1016/j.
                                                                                                                                                              1
                                                                          DOI: 10.1002/cctc.202400543).                                                perly characterised the catalyst.  This  apcata.2025.120138).

       180                                                                       Chemical Weekly  April 8, 2025      Chemical Weekly  April 8, 2025                                                                  181


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