Evidence map›Paper›PMID 35163372›Full record

ArticleInternational journal of molecular sciences2022

Synthesis of Sucrose-HDI Cooligomers: New Polyols for Novel Polyurethane Networks.

Csilla Lakatos, Marcell Árpád Kordován, Katalin Czifrák, Lajos Nagy, Bence Vadkerti, Lajos Daróczi, Miklós Zsuga, Sándor Kéki

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Bio-Based Polyurethane Networks Containing Sunflower Oil Based Polyols.International journal of molecular sciences · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Csilla LakatosDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Marcell Árpád KordovánDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Katalin CzifrákDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Lajos NagyDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Bence VadkertiDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Lajos DarócziDepartment of Solid State Physics, Faculty of Science and Technology, University of Debrecen, Bem tér 18/b, H-4026 Debrecen, Hungary.
Miklós ZsugaDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Sándor KékiDepartment of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-5274-6117

Funding

GINOP GINOP-2.3.3-15-2016-00021National Research, Development, and Innovation Office (NKFI) FK-128783Thematic Excellence Programme of the Ministry for Innovation and Technology in Hungary TKP2020-IKA-04
6 · The paper itself

Abstract

Sucrose-1,6-hexamethylene diisocyanate (HDI) cooligomers were synthesized and used as new polyols for poly(ε-caprolactone) (PCL)-based polyurethanes. The polyaddition reaction of sucrose and HDI was monitored by MALDI-TOF MS. It was found that by selecting appropriate reaction conditions, mostly linear oligomer chains containing 16 sucrose units could be obtained. For the synthesis of polyurethane networks, prepolymers were prepared by the reaction of poly(ε-caprolactone) (PCL, 10 kg/mol) with HDI or 4,4'-methylene diphenyl diisocyanate (MDI) and were reacted with sucrose-HDI cooligomers. The so-obtained sucrose-containing polyurethanes were characterized by means of attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FT IR), swelling, mechanical (uniaxial tensile tests) and differential scanning calorimetry (DSC).

Indexed as

Calorimetry, Differential ScanningIsocyanatesMaterials TestingPolyestersPolyurethanesSpectroscopy, Fourier Transform InfraredSucroseTemperature1,6-hexamethylene diisocyanateIsocyanatesPolyestersPolyurethanesSucrose1,6-hexamethylene diisocyanatechemical and physical characterizationcooligomerpolyolpoly(ε-caprolactone)sucrose

Identifiers

PMID35163372
PMCPMC8836168

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.